|
 | CGH: 3
banding: 3 |
Fang Y, Elahi A, Denley RC, Rao PH, Brennan MF, and Jhanwar SC.
Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.
Anticancer Res, 29(4) 2009, 1255-62.
(PMID 19414372)
|
|
| banding: 238 |
Poirel HA, Cairo MS, Heerema NA, Swansbury J, Auperin A, Launay E, Sanger WG, et al.
Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell non-Hodgkins lymphoma: results of the FAB/LMB 96 . . .
Leukemia, 2008.
(PMID 19020548)
|
|
| banding: 1 |
Park TS, Cheong JW, Song J, Lee KA, Lee SG, Kim J, Yoon S, Choi JR, et al.
Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine.
Cancer Genet Cytogenet, 186(1) 2008, 58-60.
(PMID 18786444)
|
|
| banding: 1 |
Suzuki N, Katsusihma H, Takeuchi K, Nakamura S, Ishizawa K, Ishii S, Moriya T, et al.
Cytogenetic abnormality 46,XX,add(21)(q11.2) in a patient with follicular dendritic cell sarcoma.
Cancer Genet Cytogenet, 186(1) 2008, 54-57.
(PMID 18786443)
|
|
| banding: 5 |
Ohyashiki K, Kodama A, and Ohyashiki JH.
Recurrent der(9;18) in essential thrombocythemia with JAK2 V617F is highly linked to myelofibrosis development.
Cancer Genet Cytogenet, 186(1) 2008, 6-11.
(PMID 18786436)
|
|
| banding: 2 |
Huh HJ, Min HC, Cho HI, Chae SL, and Lee DS.
Investigation of bone marrow involvement in malignant lymphoma using fluorescence in situ hybridization: possible utility in the detection of micrometastasis.
Cancer Genet Cytogenet, 186(1) 2008, 1-5.
(PMID 18786435)
|
|
| banding: 1 |
Park TS, Song J, Lee KA, Kim J, Kim SJ, Lee JH, Choi JR, Cheong JW, Park R, Hwang SH, et al.
Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia.
Cancer Genet Cytogenet, 185(2) 2008, 109-12.
(PMID 18722881)
|
|
| banding: 1 |
Tapinassi C, Gerbino E, Malazzi O, Micucci C, Gasparini P, Najera MJ, Calasanz MJ, et al.
A new dic(7;12)(p12.21;p12.2) chromosome aberration in a case of acute myeloid leukemia.
Cancer Genet Cytogenet, 185(2) 2008, 102-05.
(PMID 18722879)
|
|
| banding: 2 |
Lau LC, Lim P, Lim YC, Teng LM, Lim TH, Lim LC, Tan SY, Lim ST, Sanger WG, et al.
Occurrence of trisomy 12, t(14;18)(q32;q21), and t(8;14)(q24.1;q11.2) in a patient with B-cell chronic lymphocytic leukemia.
Cancer Genet Cytogenet, 185(2) 2008, 95-101.
(PMID 18722878)
|
|
| banding: 5 |
Italiano A, Ebran N, Attias R, Chevallier A, Monticelli I, Mainguene C, Benchimol D, et al.
NFIB rearrangement in superficial, retroperitoneal, and colonic lipomas with aberrations involving chromosome band 9p22.
Genes Chromosomes Cancer, 47(11) 2008, 971-77.
(PMID 18663748)
|
|
 | aCGH: 38
banding: 1 |
Starczynowski DT, Vercauteren S, Telenius A, Sung S, Tohyama K, Brooks-Wilson A, et al.
High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall . . .
Blood, 2008.
(PMID 18663149)
|
|
| banding: 1 |
Tzankov A, Sotlar K, Muhlematter D, Theocharides A, Went P, Jotterand M, Horny HP, et al.
Systemic mastocytosis with associated myeloproliferative disease and precursor B lymphoblastic leukaemia with t(13;13)(q12;q22) involving FLT3.
J Clin Pathol, 61(8) 2008, 958-61.
(PMID 18663058)
|
|
| banding: 1 |
de Oliveira FM, Falcao RP, de Figueiredo Pontes LL, Simoes BP, et al.
Insertion (15;14)(q22;q13q32) in a case of Ph+ ALL.
Cancer Genet Cytogenet, 185(1) 2008, 65-67.
(PMID 18656700)
|
|
| banding: 1 |
Cornfield DB, Gheith SM, and Friedman EL.
A third case of chronic eosinophilic leukemia with the (8;9)(p23;p24) translocation.
Cancer Genet Cytogenet, 185(1) 2008, 60-61.
(PMID 18656698)
|
|
| banding: 2 |
Aventin A, Sanchez J, Nomdedeu JF, Estany C, Forcada P, La Starza R, et al.
Novel IGHalpha translocations, t(2;14)(q14.3;q32) and t(14;17)(q32;q21), in B-cell precursor acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 185(1) 2008, 57-59.
(PMID 18656697)
|
|
| banding: 1 |
Abe S, Kameoka J, Fujiwara M, Harigae H, Sasaki O, and Miyamura K.
Trisomies 4 and 10 in acute myeloid leukemia: report of a new case.
Cancer Genet Cytogenet, 185(1) 2008, 55-56.
(PMID 18656696)
|
|
| banding: 1 |
Lee SG, Park TS, Cheong JW, Yang WI, Song J, Lee KA, Kim J, Park Y, et al.
Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature.
Cancer Genet Cytogenet, 185(1) 2008, 51-54.
(PMID 18656695)
|
|
| banding: 1 |
De Braekeleer E, Douet-Guilbert N, Le Bris MJ, Morel F, Ferec C, et al.
RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.
Cancer Genet Cytogenet, 185(1) 2008, 47-50.
(PMID 18656694)
|
|
| aCGH: 1
banding: 1 |
Baeumler J, Szuhai K, Falkenburg JH, van Schie ML, Ottmann OG, et al.
Establishment and cytogenetic characterization of a human acute lymphoblastic leukemia cell line (ALL-VG) with ETV6/ABL1 rearrangement.
Cancer Genet Cytogenet, 185(1) 2008, 37-42.
(PMID 18656692)
|
|
| banding: 4 |
Villa O, Salido M, Perez-Vila ME, Ferrer A, Arenillas L, Pedro C, Espinet B, Corzo C, et al.
Blast cells with nuclear extrusions in the form of micronuclei are associated with MYC amplification in acute myeloid leukemia.
Cancer Genet Cytogenet, 185(1) 2008, 32-36.
(PMID 18656691)
|
|
| banding: 2 |
Georgy M, Yonescu R, Griffin CA, and Batista DA.
Acute mixed lineage leukemia and a t(6;14)(q25;q32) in two adults.
Cancer Genet Cytogenet, 185(1) 2008, 28-31.
(PMID 18656690)
|
|
| banding: 2 |
Poitras JL, Dal Cin P, Aster JC, Deangelo DJ, and Morton CC.
Novel SSBP2-JAK2 fusion gene resulting from a t(5;9)(q14.1;p24.1) in pre-B acute lymphocytic leukemia.
Genes Chromosomes Cancer, 47(10) 2008, 884-89.
(PMID 18618714)
|
|
| banding: 4 |
Lee HR, Kang SH, Kang HJ, Shin HY, Ahn HS, Kim HK, Park MH, Cho HI, et al.
Lineage switch from acute myeloid leukemia to biphenotypic acute leukemia with acquisition of Philadelphia chromosome.
Cancer Genet Cytogenet, 184(2) 2008, 124-26.
(PMID 18617064)
|
|
| banding: 1 |
Villalon C, Talavera M, Sordo MT, Garcia-Sagredo JM, Lopez J, San Roman C, et al.
Association of inv(3)(q21q26) with essential thrombocythemia in transformation.
Cancer Genet Cytogenet, 184(2) 2008, 122-23.
(PMID 18617063)
|
|
| banding: 1 |
Ohsaka A, Otsubo K, Yokota H, Hisa T, Saito H, and Kozaki T.
Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia . . .
Cancer Genet Cytogenet, 184(2) 2008, 113-18.
(PMID 18617061)
|
|
| banding: 1 |
Kakihana K, Kubo F, Wakabayashi S, Kurosu T, Miki T, Murakami N, et al.
A novel variant form of MLL-ELL fusion transcript with t(11;19)(q23;p13.1) in chronic myelomonocytic leukemia transforming to acute myeloid leukemia.
Cancer Genet Cytogenet, 184(2) 2008, 109-12.
(PMID 18617060)
|
|
| banding: 2 |
Italiano A, Chambonniere ML, Attias R, Chibon F, Coindre JM, and Pedeutour F.
Monosomy 7 and absence of 12q amplification in two cases of spindle cell liposarcomas.
Cancer Genet Cytogenet, 184(2) 2008, 99-104.
(PMID 18617058)
|
|
| aCGH: 1
banding: 1 |
Krupp W, Holland H, Koschny R, Bauer M, Schober R, Kirsten H, Livrea M, et al.
Genome-wide genetic characterization of an atypical meningioma by single-nucleotide polymorphism array-based mapping and classical cytogenetics.
Cancer Genet Cytogenet, 184(2) 2008, 87-93.
(PMID 18617056)
|
|
| banding: 2 |
Richebourg S, Theisen O, Plantier I, Parry A, Soenen-Cornu V, Lepelley P, et al.
Chronic myeloproliferative disorder with t(8;22)(p11;q11) can mime clonal cytogenetic evolution of authentic chronic myelogeneous leukemia.
Genes Chromosomes Cancer, 47(10) 2008, 915-18.
(PMID 18615682)
|
|
| banding: 12 |
Stewenius Y, Jin Y, Ora I, Panagopoulos I, Moller E, Mertens F, Sandstedt B, et al.
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
Genes Chromosomes Cancer, 47(10) 2008, 845-52.
(PMID 18615675)
|
|
| banding: 1 |
Fava C and Cortes J.
Philadelphia-negative acute myeloid leukemia with new chromosomal abnormalities developing after first-line imatinib treatment for chronic phase chronic myeloid . . .
Am J Hematol, 83(9) 2008, 755.
(PMID 18615551)
|
|
| banding: 1 |
Mysorekar VV, Harish K, Kilara N, Subramanian M, and Giridhar AG.
Embryonal rhabdomyosarcoma of the chest wall: a case report and review of the literature.
Indian J Pathol Microbiol, 51(2) 2008, 274-76.
(PMID 18603708)
|
|
| banding: 1 |
Kushner BH, Laquaglia MP, Kramer K, Modak S, and Cheung NK.
Recurrent metastatic neuroblastoma followed by myelodysplastic syndrome: possible leukemogenic role of temozolomide.
Pediatr Blood Cancer, 51(4) 2008, 552-54.
(PMID 18570300)
|
|
| banding: 1 |
Qiu HR, Li JY, Miao KR, Wang R, and Xu W.
Clinical and laboratory studies of an acute promyelocytic leukemia patient with double ider(17q) chromosome aberration.
Cancer Genet Cytogenet, 184(1)(1) 2008, 74-75.
(PMID 18558295)
|
|
| banding: 3 |
Shetty S and Roland B.
Isoderivative chromosome 20 in bone marrow: three new cases.
Cancer Genet Cytogenet, 184(1) 2008, 72-73.
(PMID 18558294)
|
|
| banding: 1 |
Fujieda A, Masuya M, Kitano S, Miyazaki K, Yazaki A, Sugimoto Y, Usui E, Miyata E, et al.
Deletion of chromosome arm 15q in a case of minimally differentiated hypoplastic AML-M0.
Cancer Genet Cytogenet, 184(1) 2008, 57-61.
(PMID 18558291)
|
|
| banding: 1 |
Kokate P, Ahmad F, Dalvi R, Das BR, and Mandava S.
Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype.
Cancer Genet Cytogenet, 184(1) 2008, 52-56.
(PMID 18558290)
|
|
| banding: 1 |
Abe S, Ishikawa I, Harigae H, and Sugawara T.
A new complex translocation t(5;17;15)(q11;q21;q22) in acute promyelocytic leukemia.
Cancer Genet Cytogenet, 184(1) 2008, 44-47.
(PMID 18558288)
|
|
| CGH: 2
banding: 1 |
Faussillon M, Murakami I, Bichat M, Telvi L, Jeanpierre C, Nezelof C, Jaubert F, et al.
Molecular cytogenetic anomalies and phenotype alterations in a newly established cell line from Wilms tumor with diffuse anaplasia.
Cancer Genet Cytogenet, 184(1) 2008, 22-30.
(PMID 18558285)
|
|
| aCGH: 32
banding: 29 |
Lo KC, Chalker J, Strehl S, Neat M, Smith O, Dastugue N, Kearney L, Izraeli S, et al.
Array comparative genome hybridization analysis of acute lymphoblastic leukaemia and acute megakaryoblastic leukaemia in patients with Down syndrome.
Br J Haematol, 2008.
(PMID 18557744)
|
|
| banding: 1 |
Ida CM, Wang X, Erickson-Johnson MR, Wenger DE, Blute ML, Nascimento AG, et al.
Primary retroperitoneal lipoma: a soft tissue pathology heresy?: report of a case with classic histologic, cytogenetics, and molecular genetic features.
Am J Surg Pathol, 32(6) 2008, 951-54.
(PMID 18551755)
|
|
| banding: 1 |
Barroca H, Correia C, and Castedo S.
Cytologic and cytogenetic diagnosis of pediatric renal cell carcinoma associated with t(X;17).
Acta Cytol, 52(3)(3) 2008, 384-86.
(PMID 18540314)
|
|
| banding: 8 |
Ahmad F, Dalvi R, Chavan D, Das BR, and Mandava S.
Cytogenetic profile of acute lymphocytic leukemia patients: report of a novel translocation t(4;13) (q21 x 3; q35) from an Indian population.
Hematology, 13(1) 2008, 28-33.
(PMID 18534063)
|
|
| banding: 30 |
Gervais C, Murati A, Helias C, Struski S, Eischen A, Lippert E, Tigaud I, Penther D, et al.
Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogenetique hematologique.
Leukemia, 22(8) 2008, 1567-75.
(PMID 18528428)
|
|
| banding: 1 |
Lin YC, Liang TH, Chang HN, Lin JS, and Lin HY.
Behcet disease associated with myelodysplastic syndrome.
J Clin Rheumatol, 14(3) 2008, 169-74.
(PMID 18525438)
|
|
| CGH: 22
banding: 17 |
Gayrard N, Cacheux V, Iborra F, Mourad G, and Argiles A.
Cytogenetic studies of 24 renal epithelial tumors with von Hippel-Lindau and fragile histidine triad protein expression correlation.
Arch Pathol Lab Med, 132(6) 2008, 965-73.
(PMID 18517280)
|
|
| aCGH: 1
banding: 1 |
Bostrom H, Leuchowius KJ, Hallbook H, Nordgren A, Thorn I, Thorselius M, et al.
U-2973, a novel B-cell line established from a patient with a mature B-cell leukemia displaying concurrent t(14;18) and MYC translocation to a non-IG gene partner.
Eur J Haematol, 2008.
(PMID 18510704)
|
|
| banding: 1 |
Callera F, Lopes CO, Rosa ES, and Mulin CC.
Adult transitional pre-B acute lymphoblastic leukemia associated with ring chromosome 16.
Cancer Genet Cytogenet, 183(2) 2008, 131-32.
(PMID 18503834)
|
|
| banding: 3 |
Yonescu R, Hristov AC, Ahmad A, Overby A, Thomas GH, and Griffin CA.
Cytogenetic characterization of natural killer cell leukemia.
Cancer Genet Cytogenet, 183(2) 2008, 125-30.
(PMID 18503833)
|
|
| banding: 1 |
Kamath A, Tara H, Xiang B, Bajaj R, He W, and Li P.
Double-minute MYC amplification and deletion of MTAP, CDKN2A, CDKN2B, and ELAVL2 in an acute myeloid leukemia characterized by oligonucleotide-array comparative genomic . . .
Cancer Genet Cytogenet, 183(2) 2008, 117-20.
(PMID 18503831)
|
|
| banding: 2 |
Zamecnikova A, Al Bahar S, and Ramesh P.
Simultaneous occurrence of t(9;22)(q34;q11.2) and t(16;16)(p13;q22) in a patient with chronic myeloid leukemia in blastic phase.
Cancer Genet Cytogenet, 183(2) 2008, 109-13.
(PMID 18503829)
|
|
| banding: 1 |
Cirmena G, Aliano S, Fugazza G, Bruzzone R, Garuti A, Bocciardi R, Bacigalupo A, et al.
A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q11) in a patient with acute myeloid leukemia.
Cancer Genet Cytogenet, 183(2) 2008, 105-08.
(PMID 18503828)
|
|
| banding: 2 |
Wehle D, Yonescu R, Long PP, Gala N, Epstein J, and Griffin CA.
Fluorescence in situ hybridization of 12p in germ cell tumors using a bacterial artificial chromosome clone 12p probe on paraffin-embedded tissue: clinical test . . .
Cancer Genet Cytogenet, 183(2) 2008, 99-104.
(PMID 18503827)
|
|
| banding: 14 |
Pinheiro RF, de Sa Moreira E, Silva MR, Alberto FL, and Chauffaille Mde L.
FLT3 internal tandem duplication during myelodysplastic syndrome follow-up: a marker of transformation to acute myeloid leukemia.
Cancer Genet Cytogenet, 183(2) 2008, 89-93.
(PMID 18503825)
|
|
| banding: 13 |
Colovic M, Jankovic G, Suvajdzic N, Milic N, Dordevic V, and Jankovic S.
Thirty patients with primary plasma cell leukemia: a single center experience.
Med Oncol, 25(2) 2008, 154-60.
(PMID 18488157)
|
|
| banding: 144 |
Mertz KD, Demichelis F, Sboner A, Hirsch MS, Dal Cin P, Struckmann K, Storz M, et al.
Association of cytokeratin 7 and 19 expression with genomic stability and favorable prognosis in clear cell renal cell cancer.
Int J Cancer, 123(3) 2008, 569-76.
(PMID 18478571)
|
|
| CGH: 12
banding: 12 |
McGrattan P, Campbell S, Cuthbert R, Jones F, McMullin M, and Humphreys M.
Integration of conventional cytogenetics (G-banding), comparative genomic hybridization (CGH) and interphase fluorescence in situ hybridization (i-FISH) for the detection of genomic . . .
Journal of clinical pathology, 2008, .
(PMID 18474541)
|
|
| banding: 2 |
Yamamoto K, Yakushijin K, Nishikawa S, Minagawa K, Katayama Y, Shimoyama M, et al.
Imatinib resistance in a novel translocation der(17)t(1;17)(q25;p13) with loss of TP53 but without BCR/ABL kinase domain mutation in chronic myelogenous leukemia.
Cancer Genet Cytogenet, 183(1) 2008, 77-81.
(PMID 18474303)
|
|
| banding: 1 |
Park TS, Song J, Lee KA, Min YH, Lee SG, Park Y, Kim J, Lee EY, et al.
Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding . . .
Cancer Genet Cytogenet, 183(1) 2008, 72-76.
(PMID 18474302)
|
|
| banding: 1 |
Ikuta K, Torimoto Y, Jimbo J, Inamura J, Hosoki T, Shindo M, Sato K, Takahashi H, et al.
A novel five-way chromosomal translocation observed in chronic myelogenous leukemia.
Cancer Genet Cytogenet, 183(1) 2008, 69-71.
(PMID 18474301)
|
|
| banding: 1 |
Znoyko I, Stuart RK, Ellingham T, Winters J, Wolff DJ, and Quigley DI.
Tetraploidy and 5q deletion in myelodysplastic syndrome: a case report.
Cancer Genet Cytogenet, 183(1) 2008, 64-68.
(PMID 18474300)
|
|
| banding: 7 |
Bartuma H, Domanski HA, Von Steyern FV, Kullendorff CM, Mandahl N, et al.
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
Cancer Genet Cytogenet, 183(1) 2008, 60-63.
(PMID 18474299)
|
|
| banding: 1 |
Soler G, Radford I, Meyer C, Marschalek R, Brouzes C, Ghez D, Romana S, et al.
MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literature.
Cancer Genet Cytogenet, 183(1) 2008, 53-59.
(PMID 18474298)
|
|
| banding: 3 |
Pozdnyakova O, Stachurski D, Hutchinson L, Ramakrishnan S, and Miron PM.
Trisomy 8 in B-cell chronic lymphocytic leukemia.
Cancer Genet Cytogenet, 183(1) 2008, 49-52.
(PMID 18474297)
|
|
| banding: 3 |
Athanasiadou A, Lalayanni C, Papaioannou G, Gaitatzi M, Fassas A, et al.
Novel chromosomal aberration in Philadelphia negative cells of a patient with chronic myelogenous leukemia treated with dasatinib.
Leuk Lymphoma, 49(5)(5) 2008, 1012-13.
(PMID 18464124)
|
|
| banding: 4 |
Qian SX, Li JY, Hong M, Qiu HR, Fan L, and Xu W.
Acute myeloid leukemia in four patients with t(8;21) treated with all-trans retinoic acid as a single agent.
Leuk Lymphoma, 49(5) 2008, 998-1001.
(PMID 18464121)
|
|
| banding: 10 |
Giovanella L, Taborelli M, Ceriani L, Zucca E, Cavalli F, and Delaloye AB.
99mTc-sestamibi imaging and bone marrow karyotyping in the assessment of multiple myeloma and MGUS.
Nucl Med Commun, 29(6) 2008, 535-41.
(PMID 18458600)
|
|
 | aCGH: 45
banding: 44 |
Paulsson K, Cazier J-B, Macdougall F, Stevens J, Stasevich I, Vrcelj N, Chaplin T, et al.
Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease.
Proceedings of the National Academy of Sciences of the United States of America, 105(18) 2008, 6708-13.
(PMID 18458336)
|
|
| banding: 18 |
Tauchi H, Tomizawa D, Eguchi M, Eguchi-Ishimae M, Koh K, Hirayama M, Miyamura N, et al.
Clinical features and outcome of MLL gene rearranged acute lymphoblastic leukemia in infants with additional chromosomal abnormalities other than 11q23 translocation.
Leuk Res, 32(10) 2008, 1523-29.
(PMID 18448165)
|
|
| banding: 2 |
Regauer S, Emberger W, Reich O, and Pfragner R.
Cytogenetic analyses of two new cases of endometrial stromal sarcoma--non-random reciprocal translocation t(10;17)(q22;p13) correlates with fibrous ESS.
Histopathology, 52(6) 2008, 780-83.
(PMID 18439162)
|
|
| banding: 12 |
So CC, Wan TS, Yip SF, and Chan LC.
A dual colour dual fusion fluorescence in situ hybridisation study on the genesis of complex variant translocations in chronic myelogenous leukaemia.
Oncol Rep, 19(5) 2008, 1181-84.
(PMID 18425374)
|
|
| banding: 1 |
Nakamura Y, Takahashi N, Kakegawa E, Yoshida K, Ito Y, Kayano H, Niitsu N, Jinnai I, et al.
The GAS5 (growth arrest-specific transcript 5) gene fuses to BCL6 as a result of t(1;3)(q25;q27) in a patient with B-cell lymphoma.
Cancer Genet Cytogenet, 182(2) 2008, 144-49.
(PMID 18406879)
|
|
| banding: 1 |
Wettach GR, Boyd LJ, Lawce HJ, Magenis RE, and Mansoor A.
Cytogenetic analysis of a hemosiderotic fibrolipomatous tumor.
Cancer Genet Cytogenet, 182(2) 2008, 140-43.
(PMID 18406878)
|
|
| banding: 2 |
Ramkumar B, Chadha MK, Barcos M, Sait SN, Heyman MR, and Baer MR.
Acute promyelocytic leukemia after mitoxantrone therapy for multiple sclerosis.
Cancer Genet Cytogenet, 182(2) 2008, 126-29.
(PMID 18406875)
|
|
| banding: 1 |
Parker TM, Klaassen RJ, and Johnston DL.
Spontaneous remission of myelodysplastic syndrome with monosomy 7 in a young boy.
Cancer Genet Cytogenet, 182(2) 2008, 122-25.
(PMID 18406874)
|
|
| banding: 41 |
Richebourg S, Eclache V, Perot C, Portnoi MF, Van den Akker J, Terre C, Maareck O, et al.
Mechanisms of genesis of variant translocation in chronic myeloid leukemia are not correlated with ABL1 or BCR deletion status or response to imatinib therapy.
Cancer Genet Cytogenet, 182(2) 2008, 95-102.
(PMID 18406870)
|
|
| banding: 6 |
Hodge JC, Quade BJ, Rubin MA, Stewart EA, Dal Cin P, and Morton CC.
Molecular and cytogenetic characterization of plexiform leiomyomata provide further evidence for genetic heterogeneity underlying uterine fibroids.
Am J Pathol, 172(5) 2008, 1403-10.
(PMID 18403592)
|
|
| aCGH: 1
banding: 1 |
Schell AJ, Xu Y, Baetz T, Harrison K, Ropchan G, Lebrun D, and Feilotter H.
Primary cardiac lymphoma: molecular cytogenetic characterization of a rare entity.
Cardiovasc Pathol, 2008.
(PMID 18402841)
|
|
| banding: 4 |
Wlodarska I, Dierickx D, Vanhentenrijk V, Van Roosbroeck K, Pospisilova H, Minnei F, et al.
Translocations targeting CCND2, CCND3, and MYCN do occur in t(11;14)-negative mantle cell lymphomas.
Blood, 111(12) 2008, 5683-90.
(PMID 18391076)
|
|
| banding: 1 |
Jankovic D, Gorello P, Liu T, Ehret S, La Starza R, Desjobert C, Baty F, Brutsche M, et al.
Leukemogenic mechanisms and targets of a NUP98/HHEX fusion in acute myeloid leukemia.
Blood, 111(12) 2008, 5672-82.
(PMID 18388181)
|
|
| banding: 1 |
Brandal P, Panagopoulos I, Bjerkehagen B, Gorunova L, Skjeldal S, Micci F, et al.
Detection of a t(1;22)(q23;q12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma.
Genes Chromosomes Cancer, 47(7) 2008, 558-64.
(PMID 18383210)
|
|
| banding: 48 |
Gabrea A, Martelli ML, Qi Y, Roschke A, Barlogie B, Shaughnessy JDJ, Sawyer JR, et al.
Secondary genomic rearrangements involving immunoglobulin or MYC loci show similar prevalences in hyperdiploid and nonhyperdiploid myeloma tumors.
Genes Chromosomes Cancer, 47(7) 2008, 573-90.
(PMID 18381641)
|
|
| banding: 1 |
Shin MG, Choi HW, Kim HR, Kim MJ, Baek HJ, Han DK, Kook H, Hwang TJ, Kim HJ, Kim SH, et al.
Tetrasomy 21 as a sole acquired abnormality without GATA1 gene mutation in pediatric acute megakaryoblastic leukemia: a case report and review of the literature.
Leuk Res, 32(10) 2008, 1615-19.
(PMID 18372039)
|
|
| banding: 1 |
Hudecek M, Bartsch K, Jakel N, Heyn S, Pfannes R, Al-Ali HK, Cross M, Ponisch W, et al.
Spontaneous remission of acute myeloid leukemia relapse after hematopoietic cell transplantation in a high-risk patient with 11q23/MLL abnormality.
Acta Haematol, 119(2) 2008, 111-14.
(PMID 18367831)
|
|
| aCGH: 2
banding: 2 |
Ehemann V, Kern MA, Breinig M, Schnabel PA, Gunawan B, Schulten HJ, Schlaeger C, et al.
Establishment, characterization and drug sensitivity testing in primary cultures of human thymoma and thymic carcinoma.
Int J Cancer, 122(12) 2008, 2719-25.
(PMID 18360827)
|
|
| banding: 3 |
Vega-Ruiz A, OBrien S, Cortes J, Kebriaei P, Thomas D, Kantarjian H, et al.
Secondary myelodysplastic syndrome in a patient with Philadelphia-positive acute lymphoblastic leukemia after achieving a major molecular response with hyperCVAD plus imatinib . . .
Leuk Res, 32(9) 2008, 1468-71.
(PMID 18355919)
|
|
| banding: 29 |
Swolin B, Rodjer S, and Westin J.
Therapy-related patterns of cytogenetic abnormalities in acute myeloid leukemia and myelodysplastic syndrome post polycythemia vera: single center experience and review of . . .
Ann Hematol, 87(6) 2008, 467-74.
(PMID 18351338)
|
|
| banding: 37 |
Douet-Guilbert N, Basinko A, Morel F, Le Bris MJ, Ugo V, Morice P, Berthou C, et al.
Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and . . .
Ann Hematol, 87(7) 2008, 537-44.
(PMID 18350294)
|
|
| banding: 3 |
Flaig TW, Tangen CM, Hussain MH, Stadler WM, Raghavan D, Crawford ED, et al.
Randomization reveals unexpected acute leukemias in Southwest Oncology Group prostate cancer trial.
J Clin Oncol, 26(9) 2008, 1532-36.
(PMID 18349405)
|
|
| banding: 89 |
Nelson M, Horsman DE, Weisenburger DD, Gascoyne RD, Dave BJ, Loberiza FR, et al.
Cytogenetic abnormalities and clinical correlations in peripheral T-cell lymphoma.
Br J Haematol, 141(4) 2008, 461-69.
(PMID 18341637)
|
|
| banding: 1 |
Moller E, Stenman G, Mandahl N, Hamberg H, Molne L, van den Oord JJ, Brosjo O, et al.
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.
J Pathol, 215(1) 2008, 78-86.
(PMID 18338330)
|
|
| banding: 1 |
Curry CV, Dishop MK, Hicks MJ, Naeem R, Reed JA, and Lopez-Terrada DH.
Clear cell sarcoma of soft tissue: diagnostic utility of fluorescence in situ hybridization and reverse transcriptase polymerase chain reaction.
J Cutan Pathol, 35(4) 2008, 411-17.
(PMID 18333903)
|
|
| banding: 1 |
Wang HP, Chen ZM, Lou JY, Xu H, Yu YB, and Jin J.
Additional rearrangements affecting the derivative chromosome 9 involved in the standard Philadelphia translocation after imatinib therapy in a patient with chronic myeloid . . .
Cancer Genet Cytogenet, 182(1) 2008, 63-64.
(PMID 18328955)
|
|
| banding: 1 |
Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, et al.
Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB . . .
Cancer Genet Cytogenet, 182(1) 2008, 56-60.
(PMID 18328953)
|
|
| banding: 1 |
Stavropoulou C, Georgakakos VN, Manola KN, Pagoni M, Garofalaki M, Pantelias GE, et al.
5RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia.
Cancer Genet Cytogenet, 182(1) 2008, 50-55.
(PMID 18328952)
|
|
| banding: 1 |
Pidala J, Pinilla-Ibarz J, and Cualing HD.
A case of acute basophilic leukemia arising from chronic myelogenous leukemia with development of t(7;8)(q32;q13).
Cancer Genet Cytogenet, 182(1) 2008, 46-49.
(PMID 18328951)
|
|
| banding: 1 |
Oren H, Yilmaz S, Sercan Z, Demircioglu F, Yuksel E, and Irken G.
Isolated myelosarcoma development in an adolescent chronic myeloid leukemia patient with t(9;22)(q34;q11.2), +8, +14, +21, and der(1)(p36).
Cancer Genet Cytogenet, 182(1) 2008, 43-45.
(PMID 18328950)
|
|
| banding: 3 |
Basecke J, Podleschny M, Becker A, Seiffert E, Schwiers I, Schwiers R, Haase D, et al.
Therapy-associated genetic aberrations in patients treated for non-Hodgkin lymphoma.
Br J Haematol, 141(1) 2008, 52-59.
(PMID 18324966)
|
|
| banding: 1 |
Bozkurt SU, Berrak SG, Tugtepe H, Canpolat C, Palanduz S, and Tecimer T.
Acute megakaryoblastic leukemia mimicking small round cell tumor with novel t(1;5)(q21;p13).
APMIS, 116(2) 2008, 163-66.
(PMID 18321370)
|
|
| banding: 1 |
Moon Y, Kim M, and Park G.
Burkitt lymphoma with dual translocation of chromosome 14: a novel chromosomal abnormality of t(8;14),t(14;15).
Ann Clin Lab Sci, 38(1) 2008, 75-79.
(PMID 18316785)
|
|
| banding: 2 |
Struski S, Mauvieux L, Gervais C, Helias C, Liu KL, and Lessard M.
ETV6/GOT1 fusion in a case of t(10;12)(q24;p13)-positive myelodysplastic syndrome.
Haematologica, 93(3) 2008, 467-68.
(PMID 18310541)
|
|
| banding: 1 |
Ahmed MS, Kroft SH, Davis NB, King DM, and Cheng YC.
Long-term remission with imatinib mesylate in Philadelphia chromosome-positive AML presenting as primary extramedullary myeloid sarcoma.
Leuk Res, 32(9) 2008, 1476-79.
(PMID 18308388)
|
|
| banding: 5 |
Silva FP, Morolli B, Storlazzi CT, Zagaria A, Impera L, Klein B, Vrieling H, et al.
ETV6 mutations and loss in AML-M0.
Leukemia, 22(8) 2008, 1639-43.
(PMID 18305557)
|
|
| banding: 1 |
Gidwani P, Ramesh KH, Liu Y, and Kolb EA.
The combination of clofarabine and cytarabine in pediatric relapsed acute lymphoblastic leukemia: a case report.
Chemotherapy, 54(2) 2008, 120-24.
(PMID 18303261)
|
|
| banding: 1 |
Dunham C, Hussong J, Seiff M, Pfeifer J, and Perry A.
Primary intracerebral angiomatoid fibrous histiocytoma: report of a case with a t(12;22)(q13;q12) causing type 1 fusion of the EWS and ATF-1 genes.
Am J Surg Pathol, 32(3) 2008, 478-84.
(PMID 18300800)
|
|
| banding: 1 |
Campiotti L, Appio L, Casalone R, Righi R, Ageno W, Solbiati F, Grandi AM, et al.
Acute myeloid leukemia with associated translocation t(15;17) and 11q23/MLL abnormality.
Leuk Lymphoma, 49(3)(3) 2008, 592-95.
(PMID 18297541)
|
|
| banding: 34 |
Nahi H, Lehmann S, Bengtzen S, Jansson M, Mollgard L, Paul C, et al.
Chromosomal aberrations in 17p predict in vitro drug resistance and short overall survival in acute myeloid leukemia.
Leuk Lymphoma, 49(3) 2008, 508-16.
(PMID 18297528)
|
|
| banding: 3 |
Christie L, Kernohan N, Levison D, Sales M, Cunningham J, Gillespie K, Batstone P, et al.
C-MYC translocation in t(14;18) positive follicular lymphoma at presentation: An adverse prognostic indicator?
Leuk Lymphoma, 49(3) 2008, 470-76.
(PMID 18297523)
|
|
| banding: 2 |
Reddy KS.
Two cases assessed for myeloid disorders had an unexpected twist.
Cancer Genet Cytogenet, 181(2) 2008, 138-40.
(PMID 18295667)
|
|
| banding: 2 |
Impera L, Albano F, Mancini M, Aventin A, Rocchi M, and Storlazzi CT.
Similar mechanisms formed ring markers containing chromosome 12 pericentromeric region in two patients with therapy-related acute myeloid leukemia.
Cancer Genet Cytogenet, 181(2) 2008, 131-37.
(PMID 18295666)
|
|
| banding: 2 |
Zeidan A and Phatak P.
Acquired biclonal chromosome X aberrations without autosomal chromosomal anomalies in acute myeloid leukemia.
Cancer Genet Cytogenet, 181(2) 2008, 125-30.
(PMID 18295665)
|
|
| banding: 1 |
Rawlinson NJ, West WW, Nelson M, and Bridge JA.
Aggressive angiomyxoma with t(12;21) and HMGA2 rearrangement: report of a case and review of the literature.
Cancer Genet Cytogenet, 181(2) 2008, 119-24.
(PMID 18295664)
|
|
| CGH: 3
banding: 3 |
Shen H, Zhu Y, Wu YJ, Qiu HR, and Shu YQ.
Genomic alterations in lung adenocarcinomas detected by multicolor fluorescence in situ hybridization and comparative genomic hybridization.
Cancer Genet Cytogenet, 181(2) 2008, 100-07.
(PMID 18295661)
|
|
| banding: 1 |
Park TS, Song J, Kim JS, Yang WI, Song S, Kim SJ, Suh B, and Choi JR.
8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with . . .
Cancer Genet Cytogenet, 181(2) 2008, 93-99.
(PMID 18295660)
|
|
| aCGH: 1
banding: 1 |
Maire G, Brown CW, Bayani J, Pereira C, Gravel DH, Bell JC, Zielenska M, et al.
Complex rearrangement of chromosomes 19, 21, and 22 in Ewing sarcoma involving a novel reciprocal inversion-insertion mechanism of EWS-ERG fusion gene formation: a case analysis and . . .
Cancer Genet Cytogenet, 181(2) 2008, 81-92.
(PMID 18295659)
|
|
| banding: 3 |
Zamecnikova A, Al Bahar S, and Ramesh P.
Trisomy 6 in a CML patient receiving imatinib mesylate therapy.
Leuk Res, 32(9) 2008, 1454-57.
(PMID 18294688)
|
|
| banding: 1 |
Boils CL and Mohamed AN.
t(16;21)(q24;q22) in acute myeloid leukemia: case report and review of the literature.
Acta Haematol, 119(2) 2008, 65-68.
(PMID 18285693)
|
|
| banding: 6 |
Strehl S, Nebral K, Konig M, Harbott J, Strobl H, Ratei R, Struski S, Bielorai B, et al.
ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
Clin Cancer Res, 14(4) 2008, 977-83.
(PMID 18281529)
|
|
| banding: 1 |
Koplin SA, Twohig MH, Lund DP, and Hafez GR.
Omental lipoblastoma.
Pathol Res Pract, 204(4) 2008, 277-81.
(PMID 18276084)
|
|
| banding: 35 |
Hama A, Yagasaki H, Takahashi Y, Nishio N, Muramatsu H, Yoshida N, Tanaka M, et al.
Acute megakaryoblastic leukaemia (AMKL) in children: a comparison of AMKL with and without Down syndrome.
Br J Haematol, 140(5) 2008, 552-61.
(PMID 18275433)
|
|
| banding: 3 |
Andersen MT, Andersen MK, Christiansen DH, and Pedersen-Bjergaard J.
NPM1 mutations in therapy-related acute myeloid leukemia with uncharacteristic features.
Leukemia, 22(5) 2008, 951-55.
(PMID 18273044)
|
|
| banding: 32 |
Lugthart S, van Drunen E, van Norden Y, van Hoven A, Erpelinck CA, Valk PJ, et al.
High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated.
Blood, 111(8) 2008, 4329-37.
(PMID 18272813)
|
|
| banding: 18 |
Gmidene A, Sennana H, Elghezal H, Ziraoui S, Youssef YB, Elloumi M, Issaoui L, et al.
Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia.
Hematol Oncol, 26(2) 2008, 91-97.
(PMID 18271061)
|
|
| banding: 1 |
Shin J, Kim M, Kim DB, Yeom JO, Lee HJ, and Cho SG.
Sustained response to low-dose imatinib mesylate in a patient with chronic myelomonocytic leukemia with t(5;12)(q33;p13).
Acta Haematol, 119(1) 2008, 57-59.
(PMID 18268406)
|
|
| banding: 1 |
Kokalj Vokac N, Zagorac A, Erjavec Skerget A, Roskar Z, Podgornik H, et al.
Der(1;16)(q10;p10) in acute myeloid leukemia: the first female case described.
Acta Haematol, 119(1) 2008, 54-56.
(PMID 18268405)
|
|
| banding: 1 |
Bennour A, Sennana H, Laatiri MA, Khelif A, and Saad A.
A masked BCR/ABL rearrangement in a case of chronic myeloid leukemia with translocation t(3;9)(p14;q34).
Cancer Genet Cytogenet, 181(1) 2008, 72-74.
(PMID 18262060)
|
|
| banding: 1 |
Bettio D, Venci A, and Sarina B.
Near-tetraploid karyotype with an isochromosome 17q as the sole structural chromosomal rearrangement in a case of testicular granulocytic sarcoma.
Cancer Genet Cytogenet, 181(1) 2008, 69-71.
(PMID 18262059)
|
|
| banding: 1 |
Koitabashi M, Kanazawa T, Tamura K, Tsukada S, Suzuki M, Morikawa A, Ogawa C, et al.
A novel mutation of the SMARCB1 gene in a case of extrarenal malignant rhabdoid tumor.
Cancer Genet Cytogenet, 181(1) 2008, 67-68.
(PMID 18262058)
|
|
| banding: 1 |
Ambika S and Oo TH.
Translocation (2;7)(p11.2;q22) in a newly diagnosed low-grade B-cell non-Hodgkin lymphoma.
Cancer Genet Cytogenet, 181(1) 2008, 65-66.
(PMID 18262057)
|
|
| banding: 2 |
Torabi A, Lele SM, DiMaio D, Pinnt JC, Hess MM, Nelson M, and Bridge JA.
Lack of a common or characteristic cytogenetic anomaly in solitary fibrous tumor.
Cancer Genet Cytogenet, 181(1) 2008, 60-64.
(PMID 18262056)
|
|
| banding: 3 |
Li T, Xue Y, Zhang J, Chen S, Pan J, Wu Y, Wang Y, and Shen J.
Isodicentric 20q- in two cases of B-cell acute lymphocytic leukemia with the respective t(9;20)(p11;q11.2) and t(9;22)(q34;q11.2).
Cancer Genet Cytogenet, 181(1) 2008, 55-59.
(PMID 18262055)
|
|
| banding: 2 |
Gallagher G, Horsman DE, Tsang P, and Forrest DL.
Fusion of PRKG2 and SPTBN1 to the platelet-derived growth factor receptor beta gene (PDGFRB) in imatinib-responsive atypical myeloproliferative disorders.
Cancer Genet Cytogenet, 181(1) 2008, 46-51.
(PMID 18262053)
|
|
| banding: 1 |
Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, and Li S.
A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).
Cancer Genet Cytogenet, 181(1) 2008, 36-39.
(PMID 18262051)
|
|
| aCGH: 50
banding: 50 |
Rabin KR, Man TK, Yu A, Folsom MR, Zhao YJ, Rao PH, Plon SE, and Naeem RC.
Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia.
Pediatr Blood Cancer, 2008.
(PMID 18253961)
|
|
| banding: 1 |
Bianchini L, Maire G, Guillot B, Joujoux JM, Follana P, Simon MP, Coindre JM, et al.
Complex t(5;8) involving the CSPG2 and PTK2B genes in a case of dermatofibrosarcoma protuberans without the COL1A1-PDGFB fusion.
Virchows Arch, 452(6) 2008, 689-96.
(PMID 18253748)
|
|
| banding: 36 |
Mackinnon RN and Campbell LJ.
Dicentric chromosomes and 20q11.2 amplification in MDS/AML with apparent monosomy 20.
Cytogenet Genome Res, 119(3-4) 2007, 211-20.
(PMID 18253031)
|
|
| banding: 1 |
Herens C, Lambert F, Quintanilla-Martinez L, Bisig B, Deusings C, et al.
Cyclin D1-negative mantle cell lymphoma with cryptic t(12;14)(p13;q32) and cyclin D2 overexpression.
Blood, 111(3) 2008, 1745-46.
(PMID 18223179)
|
|
| banding: 1 |
Kusakabe M, Suzukawa K, Nanmoku T, Obara N, Okoshi Y, Mukai HY, Hasegawa Y, Kojima H, et al.
Detection of the STAT5B-RARA fusion transcript in acute promyelocytic leukemia with the normal chromosome 17 on G-banding.
Eur J Haematol, 80(5) 2008, 444-47.
(PMID 18221386)
|
|
| banding: 1 |
Henderson MJ, Choi S, Beesley AH, Baker DL, Wright D, Papa RA, Murch A, Campbell LJ, et al.
A xenograft model of infant leukaemia reveals a complex MLL translocation.
Br J Haematol, 140(6) 2008, 716-19.
(PMID 18218047)
|
|
| banding: 3 |
Shah N, Leaker MT, Teshima I, Baruchel S, Abdelhaleem M, and Ye CC.
Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia.
Pediatr Blood Cancer, 50(5) 2008, 1052-53.
(PMID 18213712)
|
|
| banding: 3 |
Nadal N, Stephan JL, Cornillon J, Guyotat D, Flandrin P, and Campos L.
RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation.
Cancer Genet Cytogenet, 180(2) 2008, 168-69.
(PMID 18206548)
|
|
| banding: 1 |
Zamecnikova A.
Small marker chromosome and monosomy 7 in a pediatric patient with MDS.
Cancer Genet Cytogenet, 180(2) 2008, 163-64.
(PMID 18206546)
|
|
| banding: 1 |
Ahmad F, Kokate P, Chheda P, Dalvi R, Das BR, and Mandava S.
Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2.
Cancer Genet Cytogenet, 180(2) 2008, 153-57.
(PMID 18206543)
|
|
| banding: 2 |
Snijder S, Mellink CH, and van der Lelie H.
Translocation (2;11)(q37;q23) in therapy-related myelodysplastic syndrome after treatment for acute promyelocytic leukemia.
Cancer Genet Cytogenet, 180(2) 2008, 149-52.
(PMID 18206542)
|
|
| banding: 2 |
Muntean A, Bergstrasser E, Diepold M, Niggli FK, and Betts DR.
Karyotypic characterization of infant embryonal rhabdomyosarcoma.
Cancer Genet Cytogenet, 180(2) 2008, 145-48.
(PMID 18206541)
|
|
| banding: 13 |
Perez-Vera P, Montero-Ruiz O, Frias S, Rivera-Luna R, Valladares A, Arenas D, et al.
Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature.
Cancer Genet Cytogenet, 180(2) 2008, 129-34.
(PMID 18206538)
|
|
| banding: 3 |
Yagyu S, Morimoto A, Kakazu N, Tamura S, Fujiki A, Nakase Y, Iehara T, Hosoi H, et al.
Late appearance of a Philadelphia chromosome in a patient with therapy-related acute myeloid leukemia and high expression of EVI1.
Cancer Genet Cytogenet, 180(2) 2008, 115-20.
(PMID 18206536)
|
|
| banding: 1 |
Bouron-Dal Soglio D, Truong F, Fetni R, Hazourli S, Champagne J, Oligny LL, et al.
A B-cell lymphoma-associated chromosomal translocation in a progressive transformation of germinal center.
Hum Pathol, 39(2) 2008, 292-97.
(PMID 18206497)
|
|
| banding: 2 |
Hidalgo-Curtis C, Chase A, Drachenberg M, Roberts MW, Finkelstein JZ, Mould S, et al.
The t(1;9)(p34;q34) and t(8;12)(p11;q15) fuse pre-mRNA processing proteins SFPQ (PSF) and CPSF6 to ABL and FGFR1.
Genes Chromosomes Cancer, 47(5) 2008, 379-85.
(PMID 18205209)
|
|
| banding: 16 |
Roche-Lestienne C, Deluche L, Corm S, Tigaud I, Joha S, Philippe N, Geffroy S, Lai JL, et al.
RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib . . .
Blood, 111(7) 2008, 3735-41.
(PMID 18202228)
|
|
| banding: 1 |
Benchetritt M, Hofman V, Long E, Odin G, Basc E, Pasquier B, Pedeutour F, et al.
Primary clear cell meningioma of the orbit mimicking a metastatic carcinoma: usefulness of immunohistochemistry and cytogenetic analysis.
Virchows Arch, 452(2) 2008, 209-13.
(PMID 18193452)
|
|
| CGH: 26
banding: 33 |
Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, et al.
Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
Neoplasma, 55(1) 2008, 23-30.
(PMID 18190236)
|
|
| CGH: 5
banding: 29 |
Micci F, Haugom L, Abeler VM, Trope CG, Danielsen HE, and Heim S.
Consistent numerical chromosome aberrations in thecofibromas of the ovary.
Virchows Arch, 2008.
(PMID 18188592)
|
|
| banding: 2 |
Zhong CH, Prima V, Liang X, Frye C, McGavran L, Meltesen L, Wei Q, Boomer T, et al.
E2A-ZNF384 and NOL1-E2A fusion created by a cryptic t(12;19)(p13.3; p13.3) in acute leukemia.
Leukemia, 22(4) 2008, 723-29.
(PMID 18185522)
|
|
| banding: 1 |
Storlazzi CT, Albano F, Guastadisegni MC, Impera L, Muhlematter D, Meyer-Monard S, et al.
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia.
Blood Cells Mol Dis, 40(3) 2008, 452-55.
(PMID 18178491)
|
|
| banding: 2 |
Jeddi R, Gouider E, Benneji H, Mnif S, Ben Abid H, Belhadjali Z, et al.
Secondary chronic myelomonocytic leukemia with monosomy 7 after successful treatment of acute promyelocytic leukemia.
Pathol Biol (Paris), 56(3) 2008, 162-63.
(PMID 18178033)
|
|
| banding: 1 |
Lahortiga I, Akin C, Cools J, Wilson TM, Mentens N, Arthur DC, Maric I, Noel P, et al.
Activity of imatinib in systemic mastocytosis with chronic basophilic leukemia and a PRKG2-PDGFRB fusion.
Haematologica, 93(1) 2008, 49-56.
(PMID 18166785)
|
|
| banding: 1 |
Udayakumar AM, Alkindi S, Pathare AV, and Raeburn JA.
Complex t(8;13;21)(q22;q14;q22)--a novel variant of t(8;21) in a patient with acute myeloid leukemia (AML-M2).
Arch Med Res, 39(2) 2008, 252-56.
(PMID 18164974)
|
|
| banding: 1 |
Nishida H, Ueno H, Park JW, and Yano T.
Isochromosome i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD).
Leuk Res, 32(8) 2008, 1325-27.
(PMID 18164759)
|
|
| banding: 1 |
Ropke A, Kalinski T, Kluba U, von Falkenhausen U, Wieacker PF, et al.
PLAG1 activation in lipoblastoma coinciding with low-level amplification of a derivative chromosome 8 with a deletion del(8)(q13q21.2).
Cytogenet Genome Res, 119(1-2) 2007, 33-38.
(PMID 18160779)
|
|
| banding: 1 |
Mozziconacci MJ, Carbuccia N, Prebet T, Charbonnier A, Murati A, Vey N, Chaffanet M, et al.
Common features of myeloproliferative disorders with t(8;9)(p12;q33) and CEP110-FGFR1 fusion: report of a new case and review of the literature.
Leuk Res, 32(8) 2008, 1304-08.
(PMID 18096225)
|
|
| banding: 6 |
Arana-Yi C, Block AW, Sait SN, Ford LA, Barcos M, and Baer MR.
Therapy-related myelodysplastic syndrome and acute myeloid leukemia following treatment of acute myeloid leukemia: possible role of cytarabine.
Leuk Res, 32(7) 2008, 1043-48.
(PMID 18093651)
|
|
| banding: 1 |
Sevilla J, Fernandez-Plaza S, Lassaletta A, Gonzalez-Vicent M, Contra T, et al.
Early acute myeloblastic leukemia treatment for childhood myelodysplastic syndrome with t(3;5) (NPM/MLF1).
J Pediatr Hematol Oncol, 29(12) 2007, 839-40.
(PMID 18090933)
|
|
| banding: 1 |
Pan Q, Zhu YJ, Gu BW, Cai X, Bai XT, Yun HY, Zhu J, Chen B, Weng L, Chen Z, Xue YQ, et al.
A new fusion gene NUP98-IQCG identified in an acute T-lymphoid/myeloid leukemia with a t(3;11)(q29q13;p15)del(3)(q29) translocation.
Oncogene, 27(24) 2008, 3414-23.
(PMID 18084320)
|
|
| banding: 2 |
Cutting R, Taj M, and Vora A.
Childhood precursor B-cell acute lymphoblastic leukaemia and monosomy 7 with phenotypic shift at relapse; evidence for the stem cell origins of monosomy 7.
Br J Haematol, 140(5) 2008, 584-86.
(PMID 18081889)
|
|
| banding: 1 |
Aguilar A, Talavera M, Villalon C, Garcia-Sagredo JM, de Leon A, Sordo T, Cabello P, et al.
Translocation (8;21)(q22;q22) without rearrangement of RUNX1 and RUNX1T1 genes in a patient with refractory anemia with excess of blasts.
Cancer Genet Cytogenet, 180(1) 2008, 85-86.
(PMID 18068542)
|
|
| banding: 1 |
Tan D, Lau LC, Teng LM, Sane S, Lim TH, and Tien SL.
Loss of the extra chromosome 21 in a patient with Down syndrome and myelodysplasia.
Cancer Genet Cytogenet, 180(1) 2008, 79-82.
(PMID 18068540)
|
|
| banding: 1 |
Panagopoulos I, Mertens F, Lofvenberg R, and Mandahl N.
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
Cancer Genet Cytogenet, 180(1) 2008, 70-73.
(PMID 18068538)
|
|
| banding: 2 |
Phan CL, Megat Baharuddin PJ, Chin LP, Zakaria Z, Yegappan S, Sathar J, Tan SM, et al.
Amplification of BCR-ABL and t(3;21) in a patient with blast crisis of chronic myelogenous leukemia.
Cancer Genet Cytogenet, 180(1) 2008, 60-64.
(PMID 18068536)
|
|
| aCGH: 1
banding: 2 |
Woo KS, Sung KS, Kim KU, Shaffer LG, and Han JY.
Characterization of complex chromosome aberrations in a recurrent meningioma combining standard cytogenetic and array comparative genomic hybridization techniques.
Cancer Genet Cytogenet, 180(1) 2008, 56-59.
(PMID 18068535)
|
|
| banding: 1 |
Helias C, Struski S, Gervais C, Leymarie V, Mauvieux L, Herbrecht R, et al.
Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and . . .
Cancer Genet Cytogenet, 180(1) 2008, 51-55.
(PMID 18068534)
|
|
| banding: 1 |
Petit A, Radford I, Waill MC, Romana S, and Berger R.
NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
Cancer Genet Cytogenet, 180(1) 2008, 43-46.
(PMID 18068532)
|
|
| banding: 2 |
Manola KN, Georgakakos VN, Margaritis D, Stavropoulou C, Panos C, Kotsianidis I, et al.
Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.
Cancer Genet Cytogenet, 180(1) 2008, 37-42.
(PMID 18068531)
|
|
| banding: 88 |
Roberts P, Burchill SA, Brownhill S, Cullinane CJ, Johnston C, Griffiths MJ, et al.
Ploidy and karyotype complexity are powerful prognostic indicators in the Ewings sarcoma family of tumors: a study by the United Kingdom Cancer Cytogenetics and the Childrens Cancer and . . .
Genes Chromosomes Cancer, 47(3) 2008, 207-20.
(PMID 18064647)
|
|
| banding: 17 |
Persson F, Winnes M, Andren Y, Wedell B, Dahlenfors R, Asp J, Mark J, Enlund F, et al.
High-resolution array CGH analysis of salivary gland tumors reveals fusion and amplification of the FGFR1 and PLAG1 genes in ring chromosomes.
Oncogene, 27(21) 2008, 3072-80.
(PMID 18059337)
|
|
| banding: 1 |
Zhu W, Sun Z, Zhai Z, Ding K, and Wu G.
A novel t(3;19)(p21;p13) in a patient with acute myelocytic leukemia.
Cancer Genet Cytogenet, 179(2) 2007, 165-66.
(PMID 18036408)
|
|
| banding: 1 |
Gohring G, Erlacher M, van Buiren M, Juttner E, Niemeyer CM, and Schlegelberger B.
Mesenteric chloroma with t(16;16) followed by acute myelomonocytic leukemia with clonal evolution.
Cancer Genet Cytogenet, 179(2) 2007, 162-64.
(PMID 18036407)
|
|
| banding: 1 |
De Braekeleer E, Douet-Guilbert N, Le Bris MJ, Morel F, and De Braekeleer M.
Translocation 3;21, trisomy 8, and duplication of the Philadelphia chromosome: a rare but recurrent cytogenetic pathway in the blastic phase of chronic myeloid leukemia.
Cancer Genet Cytogenet, 179(2) 2007, 159-61.
(PMID 18036406)
|
|
| banding: 1 |
Zhang H, Macdonald WD, Erickson-Johnson M, Wang X, Jenkins RB, et al.
Cytogenetic and molecular cytogenetic findings of intimal sarcoma.
Cancer Genet Cytogenet, 179(2) 2007, 146-49.
(PMID 18036403)
|
|
| banding: 1 |
Kenney B, Richkind KE, Friedlaender G, and Zambrano E.
Chromosomal rearrangements in lipofibromatosis.
Cancer Genet Cytogenet, 179(2) 2007, 136-39.
(PMID 18036401)
|
|
| banding: 3 |
Park TS, Song J, Lee KA, Lee SG, Yoon S, Kim JS, Lyu CJ, and Choi JR.
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 179(2) 2007, 132-35.
(PMID 18036400)
|
|
| banding: 2 |
Struski S, Helias C, Gervais C, Leymarie V, Audhuy B, Moskovtchenko P, Lutz P, et al.
Confirmation of a novel recurrent association: BCR-ABL t(9;22) and t(19;21).
Cancer Genet Cytogenet, 179(2) 2007, 127-31.
(PMID 18036399)
|
|
| banding: 1 |
Rowe D, Strain L, Lowe C, and Jones G.
A case of acute myeloid leukemia with inv(16)(p13q22) reveals a novel MYH11 breakpoint and a new CBF beta-MYH11 transcript variant.
Haematologica, 92(10) 2007, 1433-34.
(PMID 18024381)
|
|
| banding: 10 |
Le Gouill S, Talmant P, Touzeau C, Moreau A, Garand R, Juge-Morineau N, Gaillard F, et al.
The clinical presentation and prognosis of diffuse large B-cell lymphoma with t(14;18) and 8q24/c-MYC rearrangement.
Haematologica, 92(10) 2007, 1335-42.
(PMID 18024371)
|
|
| banding: 23 |
Baro C, Salido M, Espinet B, Astier L, Domingo A, Granada I, Milla F, Carrio A, et al.
New chromosomal alterations in a series of 23 splenic marginal zone lymphoma patients revealed by Spectral Karyotyping (SKY).
Leuk Res, 32(5) 2008, 727-36.
(PMID 18023866)
|
|
| banding: 1 |
Lindberg E, Persson A, Ora I, Mertens F, Englund E, and Gisselsson D.
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma.
Neuropathology, 27(6) 2007, 556-60.
(PMID 18021376)
|
|
| banding: 17 |
Panani AD.
Single chromosomal abnormalities in Philadelphia-negative chronic myeloproliferative disorders.
In Vivo, 21(5) 2007, 867-70.
(PMID 18019426)
|
|
| banding: 5 |
Blin N, Mechinaud F, Talmant P, Garand R, Boutard P, Dastugue N, McIntyre EA, et al.
Mature B-cell lymphoblastic leukemia with MLL rearrangement: an uncommon and distinct subset of childhood acute leukemia.
Leukemia, 22(5)(5) 2008, 1056-59.
(PMID 18007578)
|
|
| banding: 1 |
Soler G, Radford-Weiss I, Ben-Abdelali R, Mahlaoui N, Ponceau JF, Macintyre EA, et al.
Fusion of ZMIZ1 to ABL1 in a B-cell acute lymphoblastic leukaemia with a t(9;10)(q34;q22.3) translocation.
Leukemia, 22(6) 2008, 1278-80.
(PMID 18007576)
|
|
| banding: 1 |
Stewenius Y, Jin Y, Ora I, de Kraker J, Bras J, Frigyesi A, Alumets J, Sandstedt B, et al.
Defective chromosome segregation and telomere dysfunction in aggressive Wilms tumors.
Clin Cancer Res, 13(22 Pt 1) 2007, 6593-602.
(PMID 18006759)
|
|
| banding: 8 |
Fujimoto Y, Nomura K, Fukada S, Shimizu D, Shimura K, Matsumoto Y, Horiike S, et al.
Immunoglobulin light chain gene translocations in non-Hodgkins lymphoma as assessed by fluorescence in situ hybridisation.
Eur J Haematol, 80(2) 2008, 143-50.
(PMID 18005388)
|
|
| banding: 21 |
Fonseca I, Fonseca R, Martins C, and Soares J.
Alteration of beta-catenin localization in salivary pleomorphic adenomas is not related to t(3;8)(p21;q12) and is mainly present in non-epithelial cell types.
Histopathology, 52(2) 2008, 244-47.
(PMID 18005137)
|
|
| banding: 1 |
Alonso CN, Longo PL, Gallego MS, Medina A, and Felice MS.
A novel AF9 breakpoint in MLL-AF9-positive acute monoblastic leukemia.
Pediatr Blood Cancer, 50(4) 2008, 869-71.
(PMID 18000862)
|
|
| banding: 2 |
Bernicot I, Douet-Guilbert N, Le Bris MJ, Herry A, Morel F, and De Braekeleer M.
Molecular cytogenetics of IGH rearrangements in non-Hodgkin B-cell lymphoma.
Cytogenet Genome Res, 118(2-4) 2007, 345-52.
(PMID 18000389)
|
|
| banding: 1 |
Ganguly BB, Kadam NN, and Agarwal MB.
Conventional and fluorescence in situ hybridization analysis of three-way complex BCR-ABL rearrangement in a chronic myeloid leukemia patient.
J Cancer Res Ther, 3(2) 2007, 124-26.
(PMID 17998739)
|
|
| banding: 2 |
Sheth FJ, Sheth JJ, and Verhest A.
A three way complex translocation (4; 9; 22) in two patients with chronic myelocytic leukemia.
J Cancer Res Ther, 1(2) 2005, 108-10.
(PMID 17998637)
|
|
| banding: 1 |
Venizelos ID, Klonizakis I, Vlahaki E, Haralambidou S, Tatsiou Z, et al.
Skin relapse of acute myeloid leukemia associated with trisomy 8.
Acta Dermatovenerol Alp Panonica Adriat, 16(2) 2007, 77-80.
(PMID 17992463)
|
|
| banding: 11 |
Otero L, Ornellas MH, de Azevedo AM, Tavares Rde C, Pires V, Abdelhay E, Bouzas LF, et al.
Karyotype abnormalities and their clinical significance in a group of chronic myeloid leukemia patients treated with hematopoietic stem cell transplantation.
Sao Paulo Med J, 125(4) 2007, 246-49.
(PMID 17992398)
|
|
| banding: 1 |
Rakheja D, Goldman S, Wilson KS, Lenarsky C, Weinthal J, and Schultz RA.
Translocation (4;19)(q35;q13.1)-associated primitive round cell sarcoma: report of a case and review of the literature.
Pediatr Dev Pathol, 11(3) 2008, 239-44.
(PMID 17990934)
|
|
| banding: 24 |
Forestier E, Gauffin F, Andersen MK, Autio K, Borgstrom G, Golovleva I, Gustafsson B, et al.
Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the . . .
Genes Chromosomes Cancer, 47(2) 2008, 149-58.
(PMID 17990329)
|
|
| banding: 1 |
Bertrand P, Maingonnat C, Picquenot JM, Dastugue N, Penther D, Ysebaert L, et al.
Characterization of three t(3;8)(q27;q24) translocations from diffuse large B-cell lymphomas.
Leukemia, 22(5) 2008, 1064-67.
(PMID 17989722)
|
|
| banding: 1 |
Larmonie NS, Dik WA, Beverloo HB, van Wering ER, van Dongen JJ, et al.
BMI1 as oncogenic candidate in a novel TCRB-associated chromosomal aberration in a patient with TCRgammadelta+ T-cell acute lymphoblastic leukemia.
Leukemia, 22(6) 2008, 1266-67.
(PMID 17989714)
|
|
| banding: 18 |
Remstein ED, Law M, Mollejo M, Piris MA, Kurtin PJ, and Dogan A.
The prevalence of IG translocations and 7q32 deletions in splenic marginal zone lymphoma.
Leukemia, 22(6) 2008, 1268-72.
(PMID 17989713)
|
|
| banding: 2 |
Ishikawa M, Yagasaki F, Okamura D, Maeda T, Sugahara Y, Jinnai I, et al.
A novel gene, ANKRD28 on 3p25, is fused with NUP98 on 11p15 in a cryptic 3-way translocation of t(3;5;11)(p25;q35;p15) in an adult patient with myelodysplastic syndrome/acute myelogenous . . .
Int J Hematol, 86(3) 2007, 238-45.
(PMID 17988990)
|
|
| banding: 1 |
Al-Achkar W, Wafa A, and Nweder MS.
A complex translocation t(5;9;22) in Philadelphia cells involving the short arm of chromosome 5 in a case of chronic myelogenous leukemia.
J Exp Clin Cancer Res, 26(3) 2007, 411-15.
(PMID 17987804)
|
|
| banding: 1 |
Hamaki T, Kajiwara K, Kami M, Murashige N, Funaki M, Harima A, Kogure K, Yamada K, et al.
Donor cell-derived acute monoblastic leukemia involving MLL gene translocation in an adult patient who received umbilical cord blood transplantation.
Bone Marrow Transplant, 41(1)(1) 2008, 91-92.
(PMID 17982506)
|
|
| banding: 1 |
Takeuchi M, Katayama Y, Okamura A, Yamamoto K, Shimoyama M, and Matsui T.
Chronic myeloid leukemia with a rare variant BCR-ABL translocation: t(9;22;21)(q34;q11.2;q11.2).
Cancer Genet Cytogenet, 179(1) 2007, 85-87.
(PMID 17981222)
|
|
| banding: 1 |
Spencer DV, Cavalier M, Kalpatthi R, and Quigley DI.
Inverted and deleted chromosome 16 with deletion of 3CBFB identified by fluorescence in situ hybridization.
Cancer Genet Cytogenet, 179(1) 2007, 82-84.
(PMID 17981221)
|
|
| banding: 1 |
Yamamoto K, Ono K, Katayama Y, Shimoyama M, and Matsui T.
Derivative (3)t(3;18)(q27;q21)t(18;16)(q21;?) involving the BCL2 and BCL6 genes in follicular lymphoma with t(3;14;18)(q27;q32;q21).
Cancer Genet Cytogenet, 179(1) 2007, 69-75.
(PMID 17981218)
|
|
| banding: 10 |
Adeyinka A, Smoley S, Fink S, Sanchez J, Van Dyke DL, and Dewald G.
Isochromosome (X)(p10) in hematologic disorders: FISH study of 14 new cases show three types of centromere signal patterns.
Cancer Genet Cytogenet, 179(1) 2007, 25-30.
(PMID 17981211)
|
|
| banding: 1 |
Wang HY, Wilson KS, McKenna RW, Xu Y, and Karandikar N.
An extranodal nasal natural killer/T-cell lymphoma with isochromosome 7q10 as the sole cytogenetic aberration was initially diagnosed via bone marrow biopsy.
Arch Pathol Lab Med, 131(11) 2007, 1709-14.
(PMID 17979491)
|
|
| banding: 25 |
Najfeld V, Cozza A, Berkofsy-Fessler W, Prchal J, and Scalise A.
Numerical gain and structural rearrangements of JAK2, identified by FISH, characterize both JAK2617V>F-positive and -negative patients with Ph-negative MPD, myelodysplasia, and B-lymphoid . . .
Exp Hematol, 35(11) 2007, 1668-76.
(PMID 17976519)
|
|
| banding: 1 |
Koga Y, Matsuzaki A, Suminoe A, Washitoh N, Hara T, Hara T, Tajiri T, et al.
Treatment-related acute myelomonocytic leukemia with t(11;19) in a child following chemotherapy for hepatoblastoma.
Pediatr Blood Cancer, 50(4) 2008, 943-44.
(PMID 17973320)
|
|
| banding: 14 |
Sahin FI, Kizilkilic E, Bulakbasi T, Yilmaz Z, Boga C, Ozalp O, Karakus S, et al.
Cytogenetic findings and clinical outcomes of adult acute myeloid leukaemia patients.
Clin Exp Med, 7(3) 2007, 102-07.
(PMID 17972052)
|
|
| banding: 1 |
Chinen Y, Taki T, Nishida K, Shimizu D, Okuda T, Yoshida N, Kobayashi C, Koike K, et al.
Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(q11;q22) by bubble PCR method for . . .
Oncogene, 27(15) 2008, 2249-56.
(PMID 17968322)
|
|
| banding: 1 |
Hauer J, Tosi S, Schuster FR, Harbott J, Kolb HJ, and Borkhardt A.
Graft versus leukemia effect after haploidentical HSCT in a MLL-negative infant AML with HLXB9/ETV6 rearrangement.
Pediatr Blood Cancer, 50(4) 2008, 921-23.
(PMID 17960638)
|
|
| banding: 2 |
Frau DV, Lai ML, Caria P, Dettori T, Coni P, Faa G, Morandi L, Tallini G, et al.
Trisomy 17 as a marker for a subset of noninvasive thyroid nodules with focal features of papillary carcinoma: cytogenetic and molecular analysis of 62 cases and correlation with . . .
J Clin Endocrinol Metab, 93(1) 2008, 177-81.
(PMID 17956956)
|
|
| banding: 1 |
Udayakumar AM, Pathare AV, Alkindi S, and Raeburn JA.
Biphenotypic leukemia with interstitial del(9)(q22q32) as a sole abnormality.
Cancer Genet Cytogenet, 178(2) 2007, 170-72.
(PMID 17954277)
|
|
| banding: 1 |
Abla O, Dror Y, and Shago M.
Translocation (X;10) in a child with therapy-related acute myeloid leukemia following chemotherapy for Ewings Sarcoma.
Cancer Genet Cytogenet, 178(2) 2007, 168-69.
(PMID 17954276)
|
|
| banding: 1 |
Kenney B, Richkind KE, and Zambrano E.
Solid variant of aneurysmal bone cyst with a novel (X;9) translocation.
Cancer Genet Cytogenet, 178(2) 2007, 155-59.
(PMID 17954273)
|
|
| banding: 1 |
Abdelhaleem M, Shago M, Sayeh E, and Abla O.
Childhood myeloid/natural killer precursor acute leukemia with novel chromosomal aberrations der(5)t(4;5)(q31;q31.3) and t(14;17)(q32;q23).
Cancer Genet Cytogenet, 178(2) 2007, 141-43.
(PMID 17954270)
|
|
| banding: 3 |
Streblow RC, Dafferner AJ, Nelson M, Fletcher M, West WW, Stevens RK, Gatalica Z, et al.
Imbalances of chromosomes 4, 9, and 12 are recurrent in the thecoma-fibroma group of ovarian stromal tumors.
Cancer Genet Cytogenet, 178(2) 2007, 135-40.
(PMID 17954269)
|
|
| aCGH: 1
banding: 1 |
Holland H, Koschny R, Krupp W, Meixensberger J, Bauer M, Schober R, Kirsten H, et al.
Cytogenetic and molecular biological characterization of an adult medulloblastoma.
Cancer Genet Cytogenet, 178(2) 2007, 104-13.
(PMID 17954265)
|
|
| banding: 8 |
Panani AD.
Preferential involvement of chromosome 11 as add(11)(p15) in ovarian cancer: is it a common cytogenetic abnormality in cancer?
Cancer Lett, 258(2) 2007, 262-67.
(PMID 17945413)
|
|
| banding: 5 |
Kim M, Lim J, Kim Y, Han K, Lee DH, Chung NG, Cho B, Kim HK, Eom KS, Min CK, et al.
The genetic characterization of acute promyelocytic leukemia with cryptic t(15;17) including a new recurrent additional cytogenetic abnormality i(17)(q10).
Leukemia, 22(4) 2008, 881-83.
(PMID 17943164)
|
|
| banding: 13 |
Russell LJ, Akasaka T, Majid A, Sugimoto KJ, Loraine Karran E, Nagel I, Harder L, et al.
t(6;14)(p22;q32): a new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL).
Blood, 111(1) 2008, 387-91.
(PMID 17940204)
|
|
| banding: 1 |
Shvidel L, Sigler E, Vorst E, Feldberg E, Voskoboinic N, Shtalrid M, et al.
A novel cytogenetic aberration found in stem cell leukemia/lymphoma syndrome.
Leukemia, 22(3) 2008, 644-46.
(PMID 17928887)
|
|
| banding: 38 |
Luquet I, Lai JL, Barin C, Baranger L, Bilhou-Nabera C, Lippert E, Gervais C, et al.
Hyperdiploid karyotypes in acute myeloid leukemia define a novel entity: a study of 38 patients from the Groupe Francophone de Cytogenetique Hematologique (GFCH).
Leukemia, 22(1) 2008, 132-37.
(PMID 17928884)
|
|
| banding: 2 |
Quintas-Cardama A, Gibbons DL, Cortes J, Bobadilla D, Slovak ML, Kantarjian H, et al.
Association of 3q21q26 syndrome and late-appearing Philadelphia chromosome in acute myeloid leukemia.
Leukemia, 22(4) 2008, 877-78.
(PMID 17928880)
|
|
| banding: 9 |
Landstrom AP, Knudson RA, Dewald GW, Ketterling RP, and Tefferi A.
Philadelphia chromosome mosaicism at diagnosis in chronic myeloid leukemia: clinical correlates and effect on imatinib mesylate treatment outcome.
Leuk Lymphoma, 48(11) 2007, 2137-40.
(PMID 17926177)
|
|
| banding: 2 |
Moller E, Mandahl N, Mertens F, and Panagopoulos I.
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors.
Genes Chromosomes Cancer, 47(1) 2008, 21-25.
(PMID 17918257)
|
|
| banding: 1 |
Oliveira FM, Tone LG, Simoes BP, Rego EM, Araujo AG, and Falcao RP.
Blastoid mantle cell lymphoma with t(2;8) (p12;q24).
Leuk Lymphoma, 48(10) 2007, 2079-82.
(PMID 17917978)
|
|
| banding: 1 |
Chang ST, Hsieh YC, Lu YH, Tzeng CC, Lin CN, and Chuang SS.
Floral leukemic cells transformed from marginal zone lymphoma.
Pathol Res Pract, 204(1) 2008, 23-26.
(PMID 17913385)
|
|
| banding: 75 |
Paulsson K, Horvat A, Strombeck B, Nilsson F, Heldrup J, Behrendtz M, Forestier E, et al.
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia.
Genes Chromosomes Cancer, 47(1) 2008, 26-33.
(PMID 17910045)
|
|
| aCGH: 3
banding: 3 |
Lundin C, Heidenblad M, Strombeck B, Borg A, Hovland R, Heim S, et al.
Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 . . .
Cytogenet Genome Res, 118(1) 2007, 13-18.
(PMID 17901695)
|
|
| banding: 2 |
Nebral K, Konig M, Harder L, Siebert R, Haas OA, and Strehl S.
Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukaemia.
Br J Haematol, 139(2) 2007, 269-74.
(PMID 17897302)
|
|
| banding: 1 |
Sakamoto A, Yamamoto H, Yoshida T, Tanaka K, Matsuda S, Oda Y, Tsuneyoshi M, et al.
Desmoplastic fibroblastoma (collagenous fibroma) with a specific breakpoint of 11q12.
Histopathology, 51(6) 2007, 859-60.
(PMID 17894801)
|
|
| banding: 1 |
Katsura Y, Suzukawa K, Nanmoku T, Nemoto N, Machino T, Obara N, Okoshi Y, Mukai HY, et al.
Myelodysplastic syndrome accompanied by basophilia and eosinophilia with t(5;12)(q31;p13).
Cancer Genet Cytogenet, 178(1) 2007, 85-88.
(PMID 17889716)
|
|
| banding: 1 |
Gindina T, Kondakova E, and Mamaev N.
Supernumerary ring chromosomes accompanied with near-tetraploidy following chemotherapy and cranial radiation in a girl with a relapsed acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 178(1) 2007, 82-84.
(PMID 17889715)
|
|
| banding: 1 |
Podgornik H, Debeljak M, Zontar D, Cernelc P, Prestor VV, and Jazbec J.
RUNX1 amplification in lineage conversion of childhood B-cell acute lymphoblastic leukemia to acute myelogenous leukemia.
Cancer Genet Cytogenet, 178(1) 2007, 77-81.
(PMID 17889714)
|
|
| banding: 1 |
Iqbal J, Gupta S, Chen QH, Brody JP, and Koduru P.
Diffuse large B-cell lymphoma with a novel translocation involving BCL6.
Cancer Genet Cytogenet, 178(1) 2007, 73-76.
(PMID 17889713)
|
|
| banding: 1 |
Rodrigues EF, de Souza DC, Camargo A, Tavares Rde C, Bouzas LF, Ornellas MH, et al.
Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome.
Cancer Genet Cytogenet, 178(1) 2007, 70-72.
(PMID 17889712)
|
|
| banding: 1 |
Bizarro S, Cerveira N, Correia C, Lisboa S, Peixoto A, Norton L, et al.
Molecular characterization of a rare MLL-AF4 (MLL-AFF1) fusion rearrangement in infant leukemia.
Cancer Genet Cytogenet, 178(1) 2007, 61-64.
(PMID 17889710)
|
|
| banding: 2 |
Zhang L, Alsabeh R, Mecucci C, La Starza R, Gorello P, Lee S, Lill M, et al.
Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
Cancer Genet Cytogenet, 178(1) 2007, 42-48.
(PMID 17889707)
|
|
| banding: 36 |
Kowalski J, Morsberger LA, Blackford A, Hawkins A, Yeo CJ, Hruban RH, et al.
Chromosomal abnormalities of adenocarcinoma of the pancreas: identifying early and late changes.
Cancer Genet Cytogenet, 178(1) 2007, 26-35.
(PMID 17889705)
|
|
| banding: 6 |
Andrieux J, Roche-Lestienne C, Geffroy S, Desterke C, Grardel N, Plantier I, et al.
Bone morphogenetic protein antagonist gene NOG is involved in myeloproliferative disease associated with myelofibrosis.
Cancer Genet Cytogenet, 178(1) 2007, 11-16.
(PMID 17889703)
|
|
| banding: 1 |
Tsuji T, Yoshinaga M, Inomoto Y, Taguchi S, and Douchi T.
Aggressive angiomyxoma of the vulva with a sole t(5;8)(p15;q22) chromosome change.
Int J Gynecol Pathol, 26(4) 2007, 494-96.
(PMID 17885504)
|
|
| banding: 2 |
Takeuchi M, Nakaseko C, Miyagi S, Takeda Y, Ozawa S, Ohwada C, Cho R, Nishimura M, et al.
Clonal expansion of non-leukemic cells expressing two novel MLL-ELL variants differing in transforming activity.
Leukemia, 22(4) 2008, 861-64.
(PMID 17882281)
|
|
| banding: 23 |
Krayenbuhl N, Pravdenkova S, and Al-Mefty O.
De novo versus transformed atypical and anaplastic meningiomas: comparisons of clinical course, cytogenetics, cytokinetics, and outcome.
Neurosurgery, 61(3) 2007, 495-503; discussion 503-4.
(PMID 17881961)
|
|
| banding: 4 |
Mitsui H, Nakazawa T, Tanimura A, Karasuno T, and Hiraoka A.
Donor cell-derived chronic myeloproliferative disease with t(7;11)(p15;p15) after cord blood transplantation in a patient with Philadelphia chromosome-positive acute lymphoblastic . . .
Int J Hematol, 86(2) 2007, 192-95.
(PMID 17875537)
|
|
| banding: 1 |
Hayama M, Niitsu N, Higashihara M, Nakamine H, and Miura I.
t(6;14)(q15;q32) in a patient with CD5+CD10+ diffuse large B-cell lymphoma.
Int J Hematol, 86(2) 2007, 147-49.
(PMID 17875529)
|
|
| banding: 1 |
Xue SL, Wu DP, Sun AN, and Tang XW.
CAG regimen enables relapsed or refractory T-cell acute lymphocytic leukemia patients to achieve complete remission: a report of six cases.
Am J Hematol, 83(2) 2008, 167-70.
(PMID 17874449)
|
|
| banding: 1 |
Orciuolo E, Buda G, Galimberti S, Sordi E, Cervetti G, and Petrini M.
Concomitant appearance of trisomy 8 and isochromosome 17q in a Philadelphia-positive clone in a patient with chronic myeloid leukemia in chronic phase: an alarm for changing therapeutic . . .
Cancer Genet Cytogenet, 177(2) 2007, 166-67.
(PMID 17854678)
|
|
| banding: 1 |
Takahashi T, Watanabe M, Minato M, Yoshimoto M, and Tsujisaki M.
A novel t(12;15)(q22;q13) in a patient with acute monoblastic leukemia.
Cancer Genet Cytogenet, 177(2) 2007, 164-65.
(PMID 17854677)
|
|
| banding: 1 |
Park TS, Song J, Lee KA, Lee SG, Min YH, and Choi JR.
t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma.
Cancer Genet Cytogenet, 177(2) 2007, 158-60.
(PMID 17854675)
|
|
| banding: 1 |
Horton ES, Dobin SM, and Donner LR.
Leiomyoma of the urinary bladder: a cytogenetic study of a case.
Cancer Genet Cytogenet, 177(2) 2007, 147-48.
(PMID 17854672)
|
|
| banding: 1 |
Sait SN, Claydon MA, Conroy JM, Nowak NJ, Barcos M, and Baer MR.
Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia.
Cancer Genet Cytogenet, 177(2) 2007, 143-46.
(PMID 17854671)
|
|
| banding: 1 |
Ida CM, Rolig KA, Hulshizer RL, Van Dyke DL, Randolph JL, Jenkins RB, Nascimento AG, et al.
Myxoinflammatory fibroblastic sarcoma showing t(2;6)(q31;p21.3) as a sole cytogenetic abnormality.
Cancer Genet Cytogenet, 177(2) 2007, 139-42.
(PMID 17854670)
|
|
| banding: 1 |
Ustun C, Kalla A, Bollag RJ, Manaloo E, Kulharya A, and Jillella A.
Relapsed acute myelogenous leukemia occurring after 18 years with recurrent novel chromosomal abnormality t(18;22)(q23;q11.2).
Cancer Genet Cytogenet, 177(2) 2007, 135-38.
(PMID 17854669)
|
|
| banding: 1 |
Hameed M, Clarke K, Amer HZ, Mahmet K, and Aisner S.
Cellular angiofibroma is genetically similar to spindle cell lipoma: a case report.
Cancer Genet Cytogenet, 177(2) 2007, 131-34.
(PMID 17854668)
|
|
| banding: 2 |
Dai H, Xue Y, Pan J, Wu Y, Wang Y, Shen J, and Zhang J.
Two novel translocations disrupt the RUNX1 gene in acute myeloid leukemia.
Cancer Genet Cytogenet, 177(2) 2007, 120-24.
(PMID 17854666)
|
|
| banding: 1 |
Aliano S, Cirmena G, Garuti A, Fugazza G, Bruzzone R, Rocco I, Malacarne M, et al.
HMGA2 overexpression in polycythemia vera with t(12;21)(q14;q22).
Cancer Genet Cytogenet, 177(2) 2007, 115-19.
(PMID 17854665)
|
|
| banding: 4 |
Choi WT, Folsom MR, Azim MF, Meyer C, Kowarz E, Marschalek R, Timchenko NA, Naeem RC, et al.
C/EBPbeta suppression by interruption of CUGBP1 resulting from a complex rearrangement of MLL.
Cancer Genet Cytogenet, 177(2) 2007, 108-14.
(PMID 17854664)
|
|
| banding: 1 |
McGrattan P, Humphreys M, Hull D, and McMullin MF.
Transformation of cytogenetically normal chronic myelomonocytic leukaemia to an acute myeloid leukaemia and the emergence of a novel +13, +15 double trisomy resulting in an adverse . . .
Ulster Med J, 76(3) 2007, 131-35.
(PMID 17853637)
|
|
| banding: 1 |
Petterson TE, Bosco AA, and Cohn RJ.
Aggressive natural killer cell leukemia presenting with hemophagocytic lymphohistiocytosis.
Pediatr Blood Cancer, 50(3) 2008, 654-57.
(PMID 17853464)
|
|
| banding: 1 |
Ramanarayanan J, Mehdi S, Brodzik F, and Pasquale D.
Clonal evolution with +11q 13, t(1;7) and t(1;4) at relapse in a patient with Ph positive acute lymphocytic leukemia (ALL) treated with single agent front line imatinib followed by . . .
Hematology, 12(6) 2007, 505-09.
(PMID 17852464)
|
|
| banding: 2 |
Sahin F, Sercan Z, Ertan Y, Ocakci S, Ay E, Vural F, Yuksel E, Tombuloglu M, et al.
Rapid transformation of atypical myeloproliferative disorder with consistent t(8;13) to B-cell acute lymphoblastic leukemia: a case report.
Hematology, 12(6) 2007, 489-92.
(PMID 17852454)
|
|
| banding: 11 |
De Melo V, Vetter M, Mazzullo H, Howard JD, Betts DR, Nacheva EP, Apperley JF, et al.
A simple FISH assay for the detection of 3q26 rearrangements in myeloid malignancy.
Leukemia, 22(2)(2) 2008, 434-37.
(PMID 17851560)
|
|
| banding: 1 |
Huh J, Moon H, and Chung W.
A case of ABL deletion in a patient with precursor B cell lymphoblastic leukemia.
Ann Hematol, 87(3) 2008, 239-41.
(PMID 17846770)
|
|
| banding: 1 |
Udayakumar AM, Pathare AV, Muralitharan S, Alghzaly AA, Alkindi S, et al.
Trisomy 21 as a sole acquired abnormality in an adult Omani patient with CD7- and CD9-positive acute myeloid leukemia.
Arch Med Res, 38(7) 2007, 797-802.
(PMID 17845902)
|
|
| aCGH: 13
banding: 13 |
Evers C, Beier M, Poelitz A, Hildebrandt B, Servan K, Drechsler M, Germing U, et al.
Molecular definition of chromosome arm 5q deletion end points and detection of hidden aberrations in patients with myelodysplastic syndromes and isolated del(5q) using oligonucleotide array . . .
Genes Chromosomes Cancer, 2007.
(PMID 17823930)
|
|
| banding: 1 |
Esteyries S, Perot C, Adelaide J, Imbert M, Lagarde A, Pautas C, Olschwang S, et al.
NCOA3, a new fusion partner for MOZ/MYST3 in M5 acute myeloid leukemia.
Leukemia, 22(3) 2008, 663-65.
(PMID 17805331)
|
|
| banding: 10 |
Haferlach C, Dicker F, Schnittger S, Kern W, and Haferlach T.
Comprehensive genetic characterization of CLL: a study on 506 cases analysed with chromosome banding analysis, interphase FISH, IgV(H) status and immunophenotyping.
Leukemia, 21(12) 2007, 2442-51.
(PMID 17805327)
|
|
| banding: 1 |
Abdelhaleem M, Shago M, Beimnet K, Sayeh E, Bartakke S, and Weitzman S.
Childhood acute myeloid leukemia with hemophagocytosis by the blasts and inv(8)(p11q13) with MOZ-TIF2 fusion transcripts.
J Pediatr Hematol Oncol, 29(9) 2007, 643-45.
(PMID 17805042)
|
|
| banding: 7 |
Van Den Akker J, Coppo P, Portnoi MF, Barbu V, Bories D, and Gorin NC.
Simultaneous regression of Philadelphia chromosome and multiple nonrecurrent clonal chromosomal abnormalities with imatinib mesylate in a patient autografted 22 years before for chronic . . .
Leuk Lymphoma, 48(9) 2007, 1858-65.
(PMID 17786726)
|
|
| banding: 16 |
Uyttebroeck A, Vanhentenrijk V, Hagemeijer A, Boeckx N, Renard M, Wlodarska I, et al.
Is there a difference in childhood T-cell acute lymphoblastic leukaemia and T-cell lymphoblastic lymphoma?
Leuk Lymphoma, 48(9) 2007, 1745-54.
(PMID 17786710)
|
|
| banding: 1 |
Callet-Bauchu E, Salles G, Gazzo S, Dalle S, Berger F, and Hayette S.
Identification of a novel e8/a4 BCR/ABL fusion transcript in a case of a transformed Sezary syndrome.
Haematologica, 92(9) 2007, 1277-78.
(PMID 17768128)
|
|
| banding: 1 |
Grand FH, Iqbal S, Zhang L, Russell NH, Chase A, and Cross NC.
A constitutively active SPTBN1-FLT3 fusion in atypical chronic myeloid leukemia is sensitive to tyrosine kinase inhibitors and immunotherapy.
Exp Hematol, 35(11) 2007, 1723-27.
(PMID 17764812)
|
|
| banding: 1 |
Antonescu CR, Dal Cin P, Nafa K, Teot LA, Surti U, Fletcher CD, et al.
EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma.
Genes Chromosomes Cancer, 46(12) 2007, 1051-60.
(PMID 17724745)
|
|
| banding: 1 |
Catalano A, Dawson MA, Somana K, Opat S, Schwarer A, Campbell LJ, et al.
The PRKAR1A gene is fused to RARA in a new variant acute promyelocytic leukemia.
Blood, 110(12) 2007, 4073-76.
(PMID 17712046)
|
|
| banding: 32 |
Deininger MW, Cortes J, Paquette R, Park B, Hochhaus A, Baccarani M, Stone R, et al.
The prognosis for patients with chronic myeloid leukemia who have clonal cytogenetic abnormalities in philadelphia chromosome-negative cells.
Cancer, 110(7) 2007, 1509-19.
(PMID 17702093)
|
|
| banding: 1 |
Yenson PR, Forrest D, Schmiegelow K, and Dalal BI.
Azathioprine-associated acute myeloid leukemia in a patient with Crohns disease and thiopurine S-methyltransferase deficiency.
Am J Hematol, 83(1) 2008, 80-83.
(PMID 17696202)
|
|
| banding: 36 |
Sharathkumar A, DeCamillo D, Bhambhani K, Cushing B, Thomas R, Mohamed AN, et al.
Children with hyperdiploid but not triple trisomy (+4,+10,+17) acute lymphoblastic leukemia have an increased incidence of extramedullary relapse on current therapies: a single institution . . .
Am J Hematol, 83(1) 2008, 34-40.
(PMID 17696201)
|
|
| banding: 3 |
Almire C, Bertrand P, Ruminy P, Maingonnat C, Wlodarska I, Martin-Subero JI, et al.
PVRL2 is translocated to the TRA@ locus in t(14;19)(q11;q13)-positive peripheral T-cell lymphomas.
Genes Chromosomes Cancer, 46(11) 2007, 1011-18.
(PMID 17696193)
|
|
| banding: 1 |
Gozzetti A, Calabrese S, Raspadori D, Crupi R, Tassi M, Bocchia M, Fabbri A, et al.
Concomitant t(4;11) and t(1;19) in a patient with biphenotypic acute leukemia.
Cancer Genet Cytogenet, 177(1) 2007, 81-82.
(PMID 17693199)
|
|
| banding: 1 |
Shin MG, Lee JS, Cho D, Kim SH, Shin JH, Suh SP, Ryang DW, Sawyer JR, Kim HR, Yang DH, et al.
Adult T-cell leukemia/lymphoma with a complex karyotype and central nervous system involvement.
Cancer Genet Cytogenet, 177(1) 2007, 78-80.
(PMID 17693198)
|
|
| banding: 1 |
Basak GW, Rokicka M, Stanczak H, Wasiutynski A, and Wiktor-Jedrzejczak W.
Robertsonian translocations in stem cell recipients as a possible indication for cytogenetic analysis of family donors.
Cancer Genet Cytogenet, 177(1) 2007, 75-77.
(PMID 17693197)
|
|
| banding: 1 |
Taylan H, Kiratli H, and Aktas D.
Monosomy 7 mosaicism in metastatic choroidal melanoma.
Cancer Genet Cytogenet, 177(1) 2007, 70-72.
(PMID 17693195)
|
|
| banding: 4 |
Weisser M, Haferlach C, Haferlach T, and Schnittger S.
Feasibility of using the combined MDS-EVI1/EVI1 gene expression as an alternative molecular marker in acute myeloid leukemia: a report of four cases.
Cancer Genet Cytogenet, 177(1) 2007, 64-69.
(PMID 17693194)
|
|
| banding: 1 |
Johnsson A, Collin A, Rydholm A, Domanski HA, Mertens F, and Mandahl N.
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
Cancer Genet Cytogenet, 177(1) 2007, 59-63.
(PMID 17693193)
|
|
| banding: 1 |
Hoshino M, Ogose A, Kawashima H, Kudo N, Hotta T, Umezu H, Tohyama T, Nakade K, et al.
Malignant solitary fibrous tumor of the soft tissue: a cytogenetic study.
Cancer Genet Cytogenet, 177(1) 2007, 55-58.
(PMID 17693192)
|
|
| banding: 5 |
Kandasamy J, Smith A, Diaz S, Rose B, and OBrien C.
Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma.
Cancer Genet Cytogenet, 177(1) 2007, 1-5.
(PMID 17693184)
|
|
| banding: 1 |
Quintas-Cardama A, Kantarjian H, Abruzzo LV, and Cortes J.
Extramedullary BCR-ABL1-negative myeloid leukemia in a patient with chronic myeloid leukemia and synchronous cytogenetic abnormalities in Philadelphia-positive and -negative clones during . . .
Leukemia, 21(11) 2007, 2394-96.
(PMID 17690707)
|
|
| aCGH: 17
banding: 17 |
Lilljebjorn H, Heidenblad M, Nilsson B, Lassen C, Horvat A, Heldrup J, Behrendtz M, et al.
Combined high-resolution array-based comparative genomic hybridization and expression profiling of ETV6/RUNX1-positive acute lymphoblastic leukemias reveal a high incidence of cryptic Xq . . .
Leukemia, 2007.
(PMID 17690704)
|
|
| banding: 1 |
Gorello P, La Starza R, Brandimarte L, Trisolini SM, Pierini V, Crescenzi B, et al.
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene.
Leukemia, 22(1) 2008, 216-18.
(PMID 17690697)
|
|
| banding: 3 |
Wang L, Bhargava R, Zheng T, Wexler L, Collins MH, Roulston D, et al.
Undifferentiated small round cell sarcomas with rare EWS gene fusions: identification of a novel EWS-SP3 fusion and of additional cases with the EWS-ETV1 and EWS-FEV . . .
J Mol Diagn, 9(4) 2007, 498-509.
(PMID 17690209)
|
|
| CGH: 31
banding: 31 |
Martin CL, Reshmi SC, Ried T, Gottberg W, Wilson JW, Reddy JK, Khanna P, Johnson JT, et al.
Chromosomal imbalances in oral squamous cell carcinoma: Examination of 31 cell lines and review of the literature.
Oral Oncol, 2007.
(PMID 17681875)
|
|
| banding: 9 |
El-Sissy AH, El-Mashari MA, Bassuni WY, and El-Swaayed AF.
Aberrant lymphoid antigen expression in acute myeloid leukemia in Saudi Arabia.
J Egypt Natl Canc Inst, 18(3) 2006, 244-49.
(PMID 17671534)
|
|
| CGH: 2
banding: 1 |
Nestler U, Schmidinger A, Schulz C, Huegens-Penzel M, Gamerdinger UA, Koehler A, et al.
Glioblastoma Simultaneously Present with Meningioma - Report of Three Cases.
Zentralbl Neurochir, 2007.
(PMID 17665342)
|
|
| banding: 1 |
Oo TH.
Trisomies 3 and 18 in a newly diagnosed chronic lymphocytic leukemia.
Cancer Genet Cytogenet, 176(2) 2007, 175.
(PMID 17656265)
|
|
| banding: 1 |
Zeidan A, Kakati S, Anderson B, Barcos M, and Wetzler M.
Monosomy 7 in t(9;22)-negative cells during nilotinib therapy in an imatinib-resistant chronic myeloid leukemia case.
Cancer Genet Cytogenet, 176(2) 2007, 169-71.
(PMID 17656263)
|
|
| banding: 1 |
Li X, Yang J, Chen X, Liu J, Li H, Zheng J, He Y, Chen Z, and Huang S.
A report of early cytogenetic response to imatinib in two patients with chronic myeloid leukemia at accelerated phase and carrying the e19a2 BCR-ABL transcript.
Cancer Genet Cytogenet, 176(2) 2007, 166-68.
(PMID 17656262)
|
|
| banding: 1 |
Kawashima H, Ogose A, Umezu H, Hotta T, Tohyama T, Tsuchiya M, et al.
Ossifying fibromyxoid tumor of soft parts with clonal chromosomal aberrations.
Cancer Genet Cytogenet, 176(2) 2007, 156-60.
(PMID 17656260)
|
|
| banding: 2 |
Melichercikova J, Brezinova J, Zemanova Z, Cermak J, and Michalova K.
Molecular cytogenetic analysis of complex karyotypes with derivative chromosome der(1)t(1;5) found in two patients with myeloid leukemia.
Cancer Genet Cytogenet, 176(2) 2007, 150-55.
(PMID 17656259)
|
|
| banding: 1 |
Yamamoto K, Okamura A, Kawano H, Katayama Y, Shimoyama M, and Matsui T.
A novel t(8;18)(q13;q21) in acute monocytic leukemia evolving from constitutional trisomy 8 mosaicism.
Cancer Genet Cytogenet, 176(2) 2007, 144-49.
(PMID 17656258)
|
|
| banding: 1 |
Hidaka E, Tanaka M, Matsuda K, Ishikawa-Matsumura M, Yamauchi K, Sano K, Honda T, et al.
A complex karyotype, including a three-way translocation generating a NUP98-HOXD13 transcript, in an infant with acute myeloid leukemia.
Cancer Genet Cytogenet, 176(2) 2007, 137-43.
(PMID 17656257)
|
|
| banding: 2 |
Gerr HD, Nassin ML, Davis EM, Jayathilaka N, Neilly ME, Schlegelberger B, Zhang Y, et al.
Cytogenetic and molecular study of the PRDX4 gene in a t(X;18)(p22;q23): a cautionary tale.
Cancer Genet Cytogenet, 176(2) 2007, 131-36.
(PMID 17656256)
|
|
| banding: 1 |
Miyazaki K, Kikukawa M, Kiuchi A, Shin K, Iwamoto T, and Ohyashiki K.
Complex translocations derived stepwise from standard t(15;17) in a patient with variant acute promyelocytic leukemia.
Cancer Genet Cytogenet, 176(2) 2007, 127-30.
(PMID 17656255)
|
|
| banding: 1 |
Szuhai K, Ijszenga M, Knijnenburg J, Dijkstra S, de Schepper A, Tanke HJ, et al.
Does parosteal liposarcoma differ from other atypical lipomatous tumors/well-differentiated liposarcomas? A molecular cytogenetic study using combined multicolor COBRA-FISH karyotyping and . . .
Cancer Genet Cytogenet, 176(2) 2007, 115-20.
(PMID 17656253)
|
|
| banding: 1 |
Patel AS, Murphy KM, Hawkins AL, Cohen JS, Long PP, Perlman EJ, et al.
RANBP2 and CLTC are involved in ALK rearrangements in inflammatory myofibroblastic tumors.
Cancer Genet Cytogenet, 176(2) 2007, 107-14.
(PMID 17656252)
|
|
| banding: 26 |
Bodvarsdottir SK, Steinarsdottir M, Hilmarsdottir H, Jonasson JG, et al.
MYC amplification and TERT expression in breast tumor progression.
Cancer Genet Cytogenet, 176(2) 2007, 93-99.
(PMID 17656250)
|
|
| banding: 1 |
Medeiros F, Erickson-Johnson MR, Keeney GL, Clayton AC, Nascimento AG, Wang X, et al.
Frequency and characterization of HMGA2 and HMGA1 rearrangements in mesenchymal tumors of the lower genital tract.
Genes Chromosomes Cancer, 46(11) 2007, 981-90.
(PMID 17654722)
|
|
| banding: 120 |
Mohamed AN, Bentley G, Bonnett ML, Zonder J, and Al-Katib A.
Chromosome aberrations in a series of 120 multiple myeloma cases with abnormal karyotypes.
Am J Hematol, 82(12) 2007, 1080-87.
(PMID 17654686)
|
|
| banding: 1 |
Gomyo H, Kajimoto K, Maeda A, Mizuno I, Funada Y, Koizumi T, Fukui E, Hanioka K, et al.
t(14;18)(q32;q21)-bearing pleural MALT lymphoma with IgM paraproteinemia: value of detection of specific cytogenetic abnormalities in the differential diagnosis of MALT lymphoma and . . .
Hematology, 12(4) 2007, 315-18.
(PMID 17654058)
|
|
| banding: 1 |
Niitsu N, Nakamine H, Hagiwara Y, Tanae K, and Miura I.
The t(1;3)(p34;q27) translocation: a nonrandom BCL6 rearrangement in diffuse large B cell lymphoma.
Ann Hematol, 87(2) 2008, 151-53.
(PMID 17653714)
|
|
| banding: 3 |
Gohring G, Karow A, Steinemann D, Wilkens L, Lichter P, Zeidler C, Niemeyer C, et al.
Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis?
Ann Hematol, 86(10) 2007, 733-39.
(PMID 17653548)
|
|
| banding: 7 |
Silva FP, Lind A, Brouwer-Mandema G, Valk PJ, and Giphart-Gassler M.
Trisomy 13 correlates with RUNX1 mutation and increased FLT3 expression in AML-M0 patients.
Haematologica, 92(8) 2007, 1123-26.
(PMID 17650443)
|
|
| banding: 1 |
Schneider F, Bohlander SK, Schneider S, Papadaki C, Kakadyia P, Dufour A, Vempati S, et al.
AML1-ETO meets JAK2: clinical evidence for the two hit model of leukemogenesis from a myeloproliferative syndrome progressing to acute myeloid leukemia.
Leukemia, 21(10) 2007, 2199-201.
(PMID 17625612)
|
|
| banding: 15 |
Jabbour E, Kantarjian HM, Abruzzo LV, OBrien S, Garcia-Manero G, Verstovsek S, et al.
Chromosomal abnormalities in Philadelphia chromosome negative metaphases appearing during imatinib mesylate therapy in patients with newly diagnosed chronic myeloid leukemia in chronic . . .
Blood, 110(8) 2007, 2991-95.
(PMID 17625066)
|
|
| banding: 1 |
Ng TL, OSullivan MJ, Pallen CJ, Hayes M, Clarkson PW, Winstanley M, Sorensen PH, et al.
Ewing sarcoma with novel translocation t(2;16) producing an in-frame fusion of FUS and FEV.
J Mol Diagn, 9(4) 2007, 459-63.
(PMID 17620387)
|
|
| banding: 1 |
Han M, Rivera MN, Batten JM, Haber DA, Dal Cin P, and Iafrate AJ.
Wilms tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene.
Genes Chromosomes Cancer, 46(10) 2007, 909-13.
(PMID 17620295)
|
|
| banding: 1 |
Serra A, Schackert HK, Mohr B, Weise A, Liehr T, and Fitze G.
t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma.
J Pediatr Surg, 42(7) 2007, E23-9.
(PMID 17618868)
|
|
| banding: 1 |
Ben Barak A, Elhasid R, Ben Itzhak O, Ben Arieh Y, Zaidman I, Haimi M, Bar-Joseph G, et al.
Infant anaplastic lymphoma: case report and review of the literature.
Pediatr Hematol Oncol, 24(5) 2007, 379-85.
(PMID 17613884)
|
|
| aCGH: 10
banding: 10 |
Davidsson J, Andersson A, Paulsson K, Heidenblad M, Isaksson M, Borg A, Heldrup J, et al.
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias . . .
Hum Mol Genet, 16(18) 2007, 2215-25.
(PMID 17613536)
|
|
| banding: 13 |
Weir EG, Ali Ansari-Lari M, Batista DA, Griffin CA, Fuller S, Smith BD, et al.
Acute bilineal leukemia: a rare disease with poor outcome.
Leukemia, 21(11) 2007, 2264-70.
(PMID 17611554)
|
|
| banding: 1 |
Otero L, Moellmann AC, Pombo-de-Oliveira MS, Ornellas MH, Pires V, Bouzas LF, et al.
Additional t(1;11)(q21;q23) with mixed lineage leukemia rearrangement in T-blastic crisis of a Ph-positive chronic myeloid leukemia.
Eur J Haematol, 79(2) 2007, 179-81.
(PMID 17608714)
|
|
| banding: 4 |
Cho BS, Kim HJ, Lee S, Eom KS, Min WS, Lee JW, and Kim CC.
Successful interim therapy with imatinib prior to allogeneic stem cell transplantation in Philadelphia chromosome-positive acute myeloid leukemia.
Eur J Haematol, 79(2) 2007, 170-73.
(PMID 17608710)
|
|
| banding: 1 |
Ashihara E, Nakamura S, Inaba T, Taki T, Hayashi Y, and Shimazaki C.
A novel AF10-CALM fusion transcript in gamma/delta-T cell type lymphoblastic lymphoma.
Am J Hematol, 82(9) 2007, 859-60.
(PMID 17597474)
|
|
| banding: 7 |
Sellmann L, Gesk S, Walter C, Ritgen M, Harder L, Martin-Subero JI, Schroers R, et al.
Trisomy 19 is associated with trisomy 12 and mutated IGHV genes in B-chronic lymphocytic leukaemia.
Br J Haematol, 138(2) 2007, 217-20.
(PMID 17593029)
|
|
| banding: 1 |
Hsieh PY, Huang SI, Li DK, Mao TL, Sheu JC, and Chen CH.
Primary effusion lymphoma involving both pleural and abdominal cavities in a patient with hepatitis B virus-related liver cirrhosis.
J Formos Med Assoc, 106(6) 2007, 504-08.
(PMID 17588846)
|
|
| banding: 1 |
Leich E, Haralambieva E, Zettl A, Chott A, Rudiger T, Holler S, Muller-Hermelink HK, et al.
Tissue microarray-based screening for chromosomal breakpoints affecting the T-cell receptor gene loci in mature T-cell lymphomas.
J Pathol, 213(1) 2007, 99-105.
(PMID 17582237)
|
|
| banding: 1 |
Platzbecker U, Mohr B, von Bonin M, Binder M, Schetelig J, Ehninger G, et al.
Lenalidomide as induction therapy before allogeneic stem cell transplantation in a patient with proliferative CMML-2 and del(5q) not involving the EGR1 locus.
Leukemia, 21(11)(11) 2007, 2384-85.
(PMID 17581611)
|
|
| banding: 3 |
Navarro JT, Feliu E, Grau J, Espinet B, Colomer D, Ribera JM, Oriol A, Granada I, et al.
Monosomy 7 with severe myelodysplasia developing during imatinib treatment of Philadelphia-positive chronic myeloid leukemia: two cases with a different outcome.
Am J Hematol, 82(9) 2007, 849-51.
(PMID 17563075)
|
|
| banding: 2 |
Curtis CE, Grand FH, Musto P, Clark A, Murphy J, Perla G, Minervini MM, Stewart J, et al.
Two novel imatinib-responsive PDGFRA fusion genes in chronic eosinophilic leukaemia.
Br J Haematol, 138(1) 2007, 77-81.
(PMID 17555450)
|
|
| banding: 1 |
Corm S, Renneville A, Rad-Quesnel E, Grardel N, Preudhomme C, et al.
Successful treatment of imatinib-resistant acute megakaryoblastic leukemia with e6a2 BCR/ABL: use of dasatinib and reduced-conditioning stem-cell transplantation.
Leukemia, 21(11) 2007, 2376-77.
(PMID 17554376)
|
|
| banding: 1 |
Engsig FN, Moller MB, Hasselbalch HK, Mahdi B, and Obel N.
Extreme neutrophil granulocytosis in a patient with anaplastic large cell lymphoma of T-cell lineage.
APMIS, 115(6) 2007, 778-83.
(PMID 17550390)
|
|
| banding: 54 |
Van Den Neste E, Robin V, Francart J, Hagemeijer A, Stul M, Vandenberghe P, et al.
Chromosomal translocations independently predict treatment failure, treatment-free survival and overall survival in B-cell chronic lymphocytic leukemia patients treated with . . .
Leukemia, 21(8) 2007, 1715-22.
(PMID 17541398)
|
|
| banding: 1 |
De Braekeleer E, Douet-Guilbert N, Le Bris MJ, Berthou C, Morel F, et al.
A new partner gene fused to ABL1 in a t(1;9)(q24;q34)-associated B-cell acute lymphoblastic leukemia.
Leukemia, 21(10) 2007, 2220-21.
(PMID 17541395)
|
|
| banding: 18 |
Pospisilova H, Baens M, Michaux L, Stul M, Van Hummelen P, Van Loo P, Vermeesch J, et al.
Interstitial del(14)(q) involving IGH: a novel recurrent aberration in B-NHL.
Leukemia, 21(9) 2007, 2079-83.
(PMID 17525729)
|
|
| banding: 1 |
Gonzalez-Campora R, Rios-Martin JJ, Solorzano-Amoretti A, Vargas de los Monteros MT, et al.
Fine needle aspiration cytology of an acral myxoinflammatory fibroblastic sarcoma: case report with cytological and cytogenetic findings.
Cytopathology, 19(2) 2008, 118-23.
(PMID 17511780)
|
|
| banding: 3 |
Alfaro R, Perez-Granero A, Duran MA, Besalduch J, Rosell J, and Bernues M.
dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes.
Leuk Res, 32(1) 2008, 159-61.
(PMID 17509681)
|
|
| banding: 6 |
Ostronoff F, Bueso-Ramos C, Cortes J, and Giralt S.
Normal hematopoietic function and multiple bone marrow clonal abnormalities in a patient with acute myeloid leukemia after two mismatched stem-cell transplants with graft failure and . . .
Am J Hematol, 82(8) 2007, 744-47.
(PMID 17506066)
|
|
| banding: 7 |
El-Sissy A, El-Mashari M, Bassuni W, and El-Swaayed A.
Molecular detection of BCR/ABL fusion gene in Saudi acute lymphoblastic leukemia patients.
J Egypt Natl Canc Inst, 18(2) 2006, 109-16.
(PMID 17496935)
|
|
| banding: 45 |
Martin-Subero JI, Ibbotson R, Klapper W, Michaux L, Callet-Bauchu E, Berger F, et al.
A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation.
Leukemia, 21(7) 2007, 1532-44.
(PMID 17495977)
|
|
| banding: 12 |
Stamatoullas A, Picquenot JM, Dumesnil C, Ruminy P, Penther D, Bertrand P, Courel MN, et al.
Conventional cytogenetics of nodular lymphocyte-predominant Hodgkins lymphoma.
Leukemia, 21(9)(9) 2007, 2064-67.
(PMID 17495968)
|
|
| banding: 4 |
Seppa L, Hengartner H, Leibundgut K, Kuhne T, Niggli FK, and Betts DR.
Loss of i(8)(q10) at relapse in two cases of childhood acute myeloid leukaemia.
Leuk Lymphoma, 48(5) 2007, 1045-47.
(PMID 17487754)
|
|
| banding: 75 |
Dicker F, Haferlach C, Kern W, Haferlach T, and Schnittger S.
Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia.
Blood, 110(4) 2007, 1308-16.
(PMID 17485549)
|
|
| banding: 19 |
Cheung AM, Wan TS, Leung JC, Chan LY, Huang H, Kwong YL, Liang R, et al.
Aldehyde dehydrogenase activity in leukemic blasts defines a subgroup of acute myeloid leukemia with adverse prognosis and superior NOD/SCID engrafting potential.
Leukemia, 21(7) 2007, 1423-30.
(PMID 17476279)
|
|
| banding: 1 |
Akalin I, Kutlay NY, Ilhan O, and Tukun A.
Novel chromosomal translocations in multiple myeloma: t(13;16)(q14;q24) and t(1;15)(q10;q26).
Int J Lab Hematol, 29(3) 2007, 215-20.
(PMID 17474900)
|
|
| banding: 11 |
Porta G, Maserati E, Mattarucchi E, Minelli A, Pressato B, Valli R, Zecca M, et al.
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR.
Leukemia, 21(8) 2007, 1833-35.
(PMID 17460707)
|
|
| banding: 1 |
Cervetti G, Carulli G, Galimberti S, Azzara A, Buda G, Orciuolo E, Pelosini M, et al.
Transitory marrow aplasia during Imatinib therapy in a patient with chronic myeloid leukemia.
Leuk Res, 32(1) 2008, 194-95.
(PMID 17459473)
|
|
| banding: 1 |
Brodsky JR, Kim DY, and Jiang Z.
Cervical lipoblastoma: case report, review of literature, and genetic analysis.
Head Neck, 29(11) 2007, 1055-60.
(PMID 17427967)
|
|
| banding: 6 |
Betts DR, Stanchescu R, Niggli FK, Cohen N, Rechavi G, Amariglio N, et al.
SKY reveals a high frequency of unbalanced translocations involving chromosome 6 in t(12;21)-positive acute lymphoblastic leukemia.
Leuk Res, 32(1) 2008, 39-43.
(PMID 17418891)
|
|
| banding: 1 |
Orciuolo E, Buda G, Galimberti S, Cervetti G, Cecconi N, Papineschi F, et al.
Complex translocation t(6;9;22)(p21.1;q34;q11) at diagnosis is a therapy resistance index in chronic myeloid leukaemia.
Leuk Res, 32(1) 2008, 190-91.
(PMID 17418404)
|
|
| CGH: 1
banding: 1 |
Corral MD, Villa O, Alfaro EM, Alonso CN, Baro C, Felice MS, Rossi J, Sole F, et al.
Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2).
Pediatr Blood Cancer, 2007.
(PMID 17405156)
|
|
| banding: 2 |
Buda G, Orciuolo E, Galimberti S, Benedetti E, Caracciolo F, Cervetti G, Carulli G, et al.
Complex translocation t(3;9;22)(q21;q34;q11) at diagnosis is a negative prognostic index in chronic myeloid leukemia.
Leuk Res, 32(1) 2008, 192-94.
(PMID 17391755)
|
|
| banding: 23 |
Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, and De Braekeleer M.
Redefining monosomy 5 by molecular cytogenetics in 23 patients with MDS/AML.
Eur J Haematol, 78(6) 2007, 457-67.
(PMID 17391336)
|
|
| CGH: 1
banding: 1 |
Pelz AF, Klawunde P, Skalej M, Wieacker P, Kirches E, Schneider T, et al.
Novel chromosomal aberrations in a recurrent malignant meningioma.
Cancer Genet Cytogenet, 174(1) 2007, 48-53.
(PMID 17350466)
|
|
| banding: 1 |
Orciuolo E, Buda G, Galimberti S, Cecconi N, Cervetti G, and Petrini M.
Concomitant translocation t(14;22)(q32;q11) in a case of chronic myeloid leukemia.
Leuk Res, 32(1) 2008, 188-90.
(PMID 17346791)
|
|
| banding: 2 |
Murga Penas EM, Callet-Bauchu E, Ye H, Hinz K, Albert N, Copie-Bergman C, Gazzo S, et al.
The translocations t(6;18;11)(q24;q21;q21) and t(11;14;18)(q21;q32;q21) lead to a fusion of the API2 and MALT1 genes and occur in MALT lymphomas.
Haematologica, 92(3) 2007, 405-09.
(PMID 17339192)
|
|
| banding: 1 |
Buda G, Orciuolo E, Cecconi N, Galimberti S, Cervetti G, and Petrini M.
Poor prognosis chronic myeloid leukemia with a complex variant Philadelphia translocation, t(9;10;22)(q34;q24;q11).
Leuk Res, 31(12) 2007, 1765-66.
(PMID 17320954)
|
|
| CGH: 9
aCGH: 9
banding: 9 |
Kuchinskaya E, Nordgren A, Heyman M, Schoumans J, Corcoran M, Staaf J, Borg A, et al.
Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and . . .
Leukemia, 21(6) 2007, 1327-30.
(PMID 17315016)
|
|
| banding: 1 |
Medeiros BC, Chun K, Kamel-Reid S, and Lipton J.
Inv (11)(p15q21) in donor-derived Ph-negative cells in a patient with chronic myeloid leukemia in relapse successfully treated with imatinib mesylate post allogeneic stem cell . . .
Am J Hematol, 82(8) 2007, 758-60.
(PMID 17301975)
|
|
| banding: 1 |
La Starza R, Rosati R, Roti G, Gorello P, Bardi A, Crescenzi B, Pierini V, et al.
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome.
Leukemia, 21(4) 2007, 830-33.
(PMID 17301821)
|
|
| banding: 3 |
Walz C, Metzgeroth G, Haferlach C, Schmitt-Graeff A, Fabarius A, Hagen V, Prummer O, et al.
Characterization of three new imatinib-responsive fusion genes in chronic myeloproliferative disorders generated by disruption of the platelet-derived growth factor receptor beta . . .
Haematologica, 92(2) 2007, 163-69.
(PMID 17296564)
|
|
| banding: 5 |
Schnittger S, Bacher U, Haferlach C, Kern W, and Haferlach T.
Rare CBFB-MYH11 fusion transcripts in AML with inv(16)/t(16;16) are associated with therapy-related AML M4eo, atypical cytomorphology, atypical immunophenotype, atypical additional . . .
Leukemia, 21(4) 2007, 725-31.
(PMID 17287858)
|
|
| banding: 1 |
Reader JC, Meekins JS, Gojo I, and Ning Y.
A novel NUP98-PHF23 fusion resulting from a cryptic translocation t(11;17)(p15;p13) in acute myeloid leukemia.
Leukemia, 21(4) 2007, 842-44.
(PMID 17287853)
|
|
| banding: 1 |
Brichard B, Poirel HA, Chantrain C, Dupont S, Libouton JM, Scheiff JM, et al.
Unusual association of MLL rearrangement and secondary myelomonocytic leukemia in a 15-year-old patient treated for osteosarcoma.
Leuk Res, 31(11) 2007, 1597-99.
(PMID 17280715)
|
|
| banding: 1 |
Neumann F, Poelitz A, Hildebrandt B, Fenk R, Haas R, Royer-Pokora B, et al.
The tyrosine-kinase inhibitor imatinib induces long-term remission in a patient with chronic myelogenous leukemia with translocation t(4;22).
Leukemia, 21(4) 2007, 836-37.
(PMID 17268524)
|
|
| banding: 1 |
Williams DCJ, Massey GV, Russell EC, Riley RS, and Ben-Ezra J.
Translocation-positive acute myeloid leukemia associated with valproic acid therapy.
Pediatr Blood Cancer, 50(3) 2008, 641-43.
(PMID 17262798)
|
|
| banding: 1 |
Kreuziger LM, Porcher JC, Ketterling RP, and Steensma DP.
An MLL-SEPT9 fusion and t(11;17)(q23;q25) associated with de novo myelodysplastic syndrome.
Leuk Res, 31(8) 2007, 1145-48.
(PMID 17250889)
|
|
| CGH: 3
aCGH: 3
banding: 3 |
Meyer S, Fergusson WD, Whetton AD, Moreira-Leite F, Pepper SD, Miller C, Saunders EK, et al.
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption.
Genes Chromosomes Cancer, 46(4) 2007, 359-72.
(PMID 17243162)
|
|
| aCGH: 48
banding: 44 |
Strefford JC, Worley H, Barber K, Wright S, Stewart AR, Robinson HM, Bettney G, et al.
Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization.
Oncogene, 2007.
(PMID 17237825)
|
|
| banding: 150 |
Aamot HV, Torlakovic EE, Eide MB, Holte H, and Heim S.
Non-Hodgkin lymphoma with t(14;18): clonal evolution patterns and cytogenetic-pathologic-clinical correlations.
J Cancer Res Clin Oncol, 133(7) 2007, 455-70.
(PMID 17235551)
|
|
| banding: 2 |
Christopeit M, Mueller LP, Hainz M, Holzhausen HJ, and Behre G.
Cytogenetics detects infiltrations of a primary cutaneous acute myeloid leukemia to the kidney.
Ann Hematol, 86(4) 2007, 291-93.
(PMID 17206419)
|
|
| banding: 8 |
Inukai T, Hirose K, Inaba T, Kurosawa H, Hama A, Inada H, Chin M, Nagatoshi Y, et al.
Hypercalcemia in childhood acute lymphoblastic leukemia: frequent implication of parathyroid hormone-related peptide and E2A-HLF from translocation 17;19.
Leukemia, 21(2) 2007, 288-96.
(PMID 17183364)
|
|
| banding: 1 |
Ahmad F, Dalvi R, Mandava S, and Das BR.
Acute Myelogeneous Leukemia (M0/M1) with novel chromosomal abnormality of t(14;17) (q32; q11.2).
Am J Hematol, 82(7) 2007, 676-78.
(PMID 17177193)
|
|
| CGH: 1
aCGH: 1
banding: 1 |
Hallor KH, Heidenblad M, Brosjo O, Mandahl N, and Mertens F.
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
Cancer Genet Cytogenet, 172(1) 2007, 80-83.
(PMID 17175386)
|
|
| aCGH: 2
banding: 2 |
Schaub R, Burger A, Bausch D, Niggli FK, Schafer BW, and Betts DR.
Array comparative genomic hybridization reveals unbalanced gain of the MYCN region in Wilms tumors.
Cancer Genet Cytogenet, 172(1) 2007, 61-65.
(PMID 17175381)
|
|
| aCGH: 66
banding: 46 |
Wozniak A, Sciot R, Guillou L, Pauwels P, Wasag B, Stul M, Vermeesch JR, et al.
Array CGH analysis in primary gastrointestinal stromal tumors: cytogenetic profile correlates with anatomic site and tumor aggressiveness, irrespective of mutational . . .
Genes Chromosomes Cancer, 46(3) 2007, 261-76.
(PMID 17171690)
|
|
| banding: 8 |
Pileri SA, Ascani S, Cox MC, Campidelli C, Bacci F, Piccioli M, Piccaluga PP, et al.
Myeloid sarcoma: clinico-pathologic, phenotypic and cytogenetic analysis of 92 adult patients.
Leukemia, 21(2) 2007, 340-50.
(PMID 17170724)
|
|
| banding: 2 |
Abdelhaleem M, Beimnet K, Kirby-Allen M, Naqvi A, Hitzler J, et al.
High incidence of CALM-AF10 fusion and the identification of a novel fusion transcript in acute megakaryoblastic leukemia in children without Downs syndrome.
Leukemia, 21(2)(2) 2007, 352-53.
(PMID 17170719)
|
|
| banding: 1 |
Saitoh T, Matsushima T, Iriuchishima H, Yamane A, Irisawa H, Handa H, Tsukamoto N, et al.
Presentation of extramedullary Philadelphia chromosome-positive biphenotypic acute leukemia as testicular mass: Response to imatinib-combined chemotherapy.
Leuk Lymphoma, 47(12) 2006, 2667-69.
(PMID 17169818)
|
|
| banding: 1 |
Nayer H, Murphy KM, Hawkins AL, Long PP, Gillison M, Borowitz M, et al.
Clonal cytogenetic abnormalities and BCL2 rearrangement in interdigitating dendritic cell sarcoma.
Leuk Lymphoma, 47(12) 2006, 2651-54.
(PMID 17169812)
|
|
| banding: 2 |
Zatkova A, Fonatsch C, Sperr WR, and Valent P.
A patient with de novo AML M1 and t(16;21) with karyotype evolution.
Leuk Res, 31(9) 2007, 1319-21.
(PMID 17126398)
|
|
| banding: 2 |
Mallo M, Salido M, Espinet B, Cervera J, Canellas A, Pajuelo JC, Pedro C, Florensa L, et al.
Could ATRA/Idarubicin treatment of acute promyelocytic leukemia induce the appearance of new clonal cytogenetic abnormalities in patients in complete remission?
Leuk Res, 31(9) 2007, 1315-17.
(PMID 17092559)
|
|
| banding: 1 |
Wang L, Wang YY, Cao Q, Chen Z, and Chen SJ.
Hornerin gene was involved in a case of acute myeloid leukemia transformed from myelodysplastic syndrome with t(1;2)(q21;q37).
Leukemia, 20(12) 2006, 2184-87.
(PMID 17051244)
|
|
| banding: 1 |
De Keersmaecker K, Lahortiga I, Graux C, Marynen P, Maertens J, Cools J, et al.
Transition from EML1-ABL1 to NUP214-ABL1 positivity in a patient with acute T-lymphoblastic leukemia.
Leukemia, 20(12) 2006, 2202-04.
(PMID 17024111)
|
|
| banding: 7 |
Schoumans J, Johansson B, Corcoran M, Kuchinskaya E, Golovleva I, Grander D, et al.
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered . . .
Br J Haematol, 135(4) 2006, 492-99.
(PMID 16999846)
|
|
| banding: 4 |
Paulsson K, Heidenblad M, Morse H, Borg A, Fioretos T, and Johansson B.
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
Leukemia, 20(11) 2006, 2002-07.
(PMID 16990785)
|
|
| aCGH: 48
banding: 25 |
Mestre-Escorihuela C, Rubio-Moscardo F, Richter JA, Siebert R, Climent J, Fresquet V, et al.
Homozygous deletions localize novel tumor suppressor genes in B-cell lymphomas.
Blood, 109(1) 2007, 271-80.
(PMID 16960149)
|
|
| banding: 1 |
Mark HF, Sotomayor EA, Nelson M, Chaves F, Sanger WG, Kaleem Z, et al.
Chronic idiopathic myelofibrosis (CIMF) resulting from a unique 3;9 translocation disrupting the janus kinase 2 (JAK2) gene.
Exp Mol Pathol, 81(3) 2006, 217-23.
(PMID 16959246)
|
|
| banding: 1 |
Panagopoulos I, Lilljebjorn H, Strombeck B, Hjorth L, Olofsson T, et al.
MLL/GAS7 fusion in a pediatric case of t(11;17)(q23;p13)-positive precursor B-cell acute lymphoblastic leukemia.
Haematologica, 91(9) 2006, 1287-88.
(PMID 16956839)
|
|
| banding: 12 |
Adam P, Steinlein C, Schmid M, Haralambieva E, Stocklein H, Leich E, Rosenwald A, et al.
Characterization of chromosomal aberrations in diffuse large B-cell lymphoma (DLBL) by G-banding and spectral karyotyping (SKY).
Cytogenet Genome Res, 114(3-4) 2006, 274-78.
(PMID 16954666)
|
|
| banding: 1 |
Mkrtchyan H, Glaser M, Gross M, Wedding U, Hoffken K, Liehr T, Karst C, et al.
Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2).
Cytogenet Genome Res, 114(3-4) 2006, 270-73.
(PMID 16954665)
|
|
| banding: 1 |
Roche-Lestienne C, Dastugue N, Richebourg S, Roquefeuil B, Dalle JH, Lai JL, et al.
Acute megakaryoblastic leukemia with der(7)t(5;7)(q11;p11 approximately p12) associated with Down syndrome: a fourth case report.
Cancer Genet Cytogenet, 169(2) 2006, 184-86.
(PMID 16938582)
|
|
| banding: 1 |
Pinheiro RF, Chauffaille Mde L, and Silva MR.
A rare case of acute myeloid leukemia evolving from a myelodysplastic syndrome with der(19)t(1;19).
Cancer Genet Cytogenet, 169(2) 2006, 181-83.
(PMID 16938581)
|
|
| banding: 6 |
Davidsson J, Heidenblad M, Borg A, and Johansson B.
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
Cancer Genet Cytogenet, 169(2) 2006, 179-80.
(PMID 16938580)
|
|
| banding: 1 |
Collado R, Hueso J, Cabello AI, Oliver I, Egea M, Orero M, Miguel-Sosa A, Cigudosa JC, et al.
New translocations in a case of atypical B-cell chronic lymphocytic leukemia: involvement of ATM, MLL, and TP53 genes.
Cancer Genet Cytogenet, 169(2) 2006, 176-78.
(PMID 16938579)
|
|
| banding: 1 |
Nadal N, Flandrin P, Cornillon J, Delabesse E, Mauvieux L, Olaru D, Morel S, et al.
Successful treatment with imatinib mesylate in a case of chronic myeloproliferative disorder with a t(5;12)(q33;p13.1) without eosinophilia.
Cancer Genet Cytogenet, 169(2) 2006, 174-75.
(PMID 16938578)
|
|
| banding: 1 |
Zhang L, Kern WF, Yu Z, Mulvihill JJ, and Li S.
Cryptic and complex chromosomal rearrangements and the deletion of TP53 gene in a patient with leukemic mantle cell lymphoma.
Cancer Genet Cytogenet, 169(2) 2006, 169-73.
(PMID 16938577)
|
|
| banding: 1 |
Tsarouha H, Kyriazoglou AI, Ribeiro FR, Teixeira MR, Agnantis N, et al.
Chromosome analysis and molecular cytogenetic investigations of an epithelioid hemangioendothelioma.
Cancer Genet Cytogenet, 169(2) 2006, 164-68.
(PMID 16938576)
|
|
| banding: 7 |
Pan J, Xue Y, Wu Y, Wang Y, and Shen J.
Dicentric (7;9)(p11;p11) is a rare but recurrent abnormality in acute lymphoblastic leukemia: a study of 7 cases.
Cancer Genet Cytogenet, 169(2) 2006, 159-63.
(PMID 16938575)
|
|
| banding: 11 |
Saez B, Martin-Subero JI, Largo C, Martin MC, Odero MD, Prosper F, Siebert R, et al.
Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization . . .
Cancer Genet Cytogenet, 169(2) 2006, 143-49.
(PMID 16938572)
|
|
| banding: 7 |
Stasevich I, Utskevich R, Kustanovich A, Litvinko N, Savitskaya T, Chernyavskaya S, et al.
Translocation (10;11)(p12;q23) in childhood acute myeloid leukemia: incidence and complex mechanism.
Cancer Genet Cytogenet, 169(2) 2006, 114-20.
(PMID 16938568)
|
|
| banding: 1 |
Helbig G, Stella-Holowiecka B, Bober G, Majewski M, Grzegorczyk J, Wozniczka K, et al.
The achievement of complete molecular remission after autologous stem cell transplantation for T-cell lymphoma with associated hypereosinophilia, rare aberration t(6;11) and elevated IL-4 . . .
Haematologica, 91(8 Suppl) 2006, ECR42.
(PMID 16923526)
|
|
| banding: 1 |
Babu Rao V, Kerketta L, Madkaikar M, Farah J, and Ghosh K.
Hybrid cytogenetics of chronic lymphocytic leukemia and follicular cell lymphoma in a case of non-Hodgkins lymphoma.
Acta Haematol, 116(2) 2006, 150-52.
(PMID 16914914)
|
|
| banding: 2 |
Duell T, Poleck-Dehlin B, Schmid C, Wunderlich B, Ledderose G, Mittermuller J, et al.
Clonal karyotype evolution involving ring chromosome 1 with myelodysplastic syndrome subtype RAEB-t progressing into acute leukemia.
Acta Haematol, 116(2) 2006, 131-36.
(PMID 16914909)
|
|
| banding: 1 |
Tadmor T, Vadazs Z, Dar H, Laor R, and Attias D.
Hemophagocytic syndrome preceding acute myeloid leukemia with der t [7:17][q12; q11], monosomy, 17 and 5p-.
J Pediatr Hematol Oncol, 28(8) 2006, 544-46.
(PMID 16912598)
|
|
| banding: 5 |
Kim IS, Kim HJ, Yoo KH, Sung KW, and Kim SH.
A boy with acute lymphoblastic leukemia acquired clonal and nonclonal cytogenetic abnormalities including del(7q) and del(20q) without clinical evidence of disease after sex-mismatched cord . . .
J Pediatr Hematol Oncol, 28(8) 2006, 540-43.
(PMID 16912597)
|
|
| banding: 10 |
Strehl S, Konig M, Meyer C, Schneider B, Harbott J, Jager U, von Bergh AR, et al.
Molecular dissection of t(11;17) in acute myeloid leukemia reveals a variety of gene fusions with heterogeneous fusion transcripts and multiple splice variants.
Genes Chromosomes Cancer, 45(11) 2006, 1041-49.
(PMID 16897742)
|
|
| banding: 1 |
Talmon GA and Cohen SM.
Mesenchymal hamartoma of the liver with an interstitial deletion involving chromosome band 19q13.4: a theory as to pathogenesis?
Arch Pathol Lab Med, 130(8) 2006, 1216-18.
(PMID 16879027)
|
|
| banding: 3 |
Alimena G, Breccia M, Latagliata R, Carmosino I, Russo E, Biondo F, Diverio D, et al.
Sudden blast crisis in patients with Philadelphia chromosome-positive chronic myeloid leukemia who achieved complete cytogenetic remission after imatinib therapy.
Cancer, 107(5) 2006, 1008-13.
(PMID 16878324)
|
|
| banding: 1 |
Pullarkat V, Bedell V, Kim Y, Bhatia R, Nakamura R, Forman S, Sun J, Senitzer D, et al.
Neoplastic mast cells in systemic mastocytosis associated with t(8;21) acute myeloid leukemia are derived from the leukemic clone.
Leuk Res, 31(2) 2007, 261-65.
(PMID 16876862)
|
|
| banding: 1 |
Gozzetti A, Calabrese S, Crupi R, Tozzuoli D, Bocchia M, Fabbri A, Pirrotta MT, et al.
Trisomy 22 as sole cytogenetic abnormality in acute monoblastic leukemia (M5b).
Cancer Genet Cytogenet, 169(1) 2006, 86.
(PMID 16875946)
|
|
| banding: 1 |
Soares EM, Santos N, de Araujo Silva Amaral B, Silva ML, Leite EP, Silva MO, Muniz MT, et al.
Secondary acute myeloid leukemia with a t(1;11)(q23;p15) in an adolescent treated for testicular sarcoma.
Cancer Genet Cytogenet, 169(1) 2006, 83-85.
(PMID 16875945)
|
|
| banding: 1 |
Kim IS, Kim HJ, Choung HS, Jung CW, Kim JW, and Kim SH.
PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasm.
Cancer Genet Cytogenet, 169(1) 2006, 81-82.
(PMID 16875944)
|
|
| banding: 1 |
Manor E, Bellaiche E, and Bodner L.
Cytogenetic findings of a primary Merkel cell carcinoma.
Cancer Genet Cytogenet, 169(1) 2006, 78-80.
(PMID 16875943)
|
|
| banding: 1 |
Angelidis P, Kojouri K, Lee J, Kern W, Mulvihill JJ, and Li S.
Trisomy 1q in a patient with severe aplastic anemia.
Cancer Genet Cytogenet, 169(1) 2006, 73-75.
(PMID 16875941)
|
|
| banding: 1 |
Liu YC, Miyazawa K, Sashida G, Kodama A, and Ohyashiki K.
Deletion (20q) as the sole abnormality in Waldenstrom macroglobulinemia suggests distinct pathogenesis of 20q11 anomaly.
Cancer Genet Cytogenet, 169(1) 2006, 69-72.
(PMID 16875940)
|
|
| banding: 1 |
Morrissette JJ, Halligan GE, Punnett HH, McKenzie AS, Guerrero F, et al.
Down syndrome with low hypodiploidy in precursor B-cell acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 169(1) 2006, 58-61.
(PMID 16875938)
|
|
| banding: 9 |
Raimondi SC, Zhou Y, Shurtleff SA, Rubnitz JE, Pui CH, and Behm FG.
Near-triploidy and near-tetraploidy in childhood acute lymphoblastic leukemia: association with B-lineage blast cells carrying the ETV6-RUNX1 fusion, T-lineage immunophenotype, and favorable . . .
Cancer Genet Cytogenet, 169(1) 2006, 50-57.
(PMID 16875937)
|
|
| banding: 10 |
Assumpcao PP, Ishak G, Chen ES, Takeno SS, Leal MF, Guimaraes AC, Calcagno DQ, et al.
Numerical aberrations of chromosome 8 detected by conventional cytogenetics and fluorescence in situ hybridization in individuals from northern Brazil with gastric . . .
Cancer Genet Cytogenet, 169(1) 2006, 45-49.
(PMID 16875936)
|
|
| banding: 1 |
Ninomiya M, Abe A, Yokozawa T, Ozeki K, Yamamoto K, Ito M, Ito M, Kiyoi H, Emi N, et al.
Establishment of a myeloid leukemia cell line, TRL-01, with MLL-ENL fusion gene.
Cancer Genet Cytogenet, 169(1) 2006, 1-11.
(PMID 16875930)
|
|
| banding: 21 |
Keller CE, Nandula S, Vakiani E, Alobeid B, Murty VV, and Bhagat G.
Intrachromosomal rearrangement of chromosome 3q27: an under recognized mechanism of BCL6 translocation in B-cell non-Hodgkin lymphoma.
Hum Pathol, 37(8) 2006, 1093-99.
(PMID 16867873)
|
|
| banding: 1 |
Lopez-Gines C, Cerda-Nicolas M, Gil-Benso R, Pellin A, Lopez-Guerrero JA, Benito R, et al.
Primary glioblastoma with EGFR amplification and a ring chromosome 7 in a young patient.
Clin Neuropathol, 25(4) 2006, 193-99.
(PMID 16866301)
|
|
| CGH: 11
aCGH: 10
banding: 20 |
Bosga-Bouwer AG, Kok K, Booman M, Boven L, van der Vlies P, van den Berg A, et al.
Array comparative genomic hybridization reveals a very high frequency of deletions of the long arm of chromosome 6 in testicular lymphoma.
Genes Chromosomes Cancer, 45(10) 2006, 976-81.
(PMID 16865685)
|
|
| CGH: 60
aCGH: 60
banding: 112 |
Rucker FG, Bullinger L, Schwaenen C, Lipka DB, Wessendorf S, Frohling S, Bentz M, et al.
Disclosure of candidate genes in acute myeloid leukemia with complex karyotypes using microarray-based molecular characterization.
J Clin Oncol, 24(24) 2006, 3887-94.
(PMID 16864856)
|
|
| banding: 1 |
Gesk S, Klapper W, Martin-Subero JI, Nagel I, Harder L, Fu K, Bernd HW, et al.
A chromosomal translocation in cyclin D1-negative/cyclin D2-positive mantle cell lymphoma fuses the CCND2 gene to the IGK locus.
Blood, 108(3) 2006, 1109-10.
(PMID 16861358)
|
|
| banding: 3 |
Nguyen TT, Ma LN, Slovak ML, Bangs CD, Cherry AM, and Arber DA.
Identification of novel Runx1 (AML1) translocation partner genes SH3D19, YTHDf2, and ZNF687 in acute myeloid leukemia.
Genes Chromosomes Cancer, 45(10) 2006, 918-32.
(PMID 16858696)
|
|
| banding: 1 |
de Leval L, Harris NL, Lampertz S, and Herens C.
T-cell/histiocyte-rich large B-cell lymphoma associated with a near-tetraploid karyotype and complex genetic abnormalities.
APMIS, 114(6) 2006, 474-78.
(PMID 16856972)
|
|
| banding: 2 |
Anwar Iqbal M, Al-Omar HM, Owaidah T, Al-Humaidan H, Bhuiyan ZA, et al.
del(6)(p23) in two cases of de novo AML--a new recurrent primary chromosome abnormality.
Eur J Haematol, 77(3) 2006, 245-50.
(PMID 16856925)
|
|
| banding: 1 |
Walz C, Curtis C, Schnittger S, Schultheis B, Metzgeroth G, Schoch C, Lengfelder E, et al.
Transient response to imatinib in a chronic eosinophilic leukemia associated with ins(9;4)(q33;q12q25) and a CDK5RAP2-PDGFRA fusion gene.
Genes Chromosomes Cancer, 45(10) 2006, 950-56.
(PMID 16845659)
|
|
| banding: 1 |
Roche-Lestienne C, Richebourg S, Lai JL, Andrieux J, Soenen-Cornu V, et al.
Isolated tetrasomy 13: a fifth case report of a rare chromosome abnormality associated with poorly differentiated acute myeloid leukemia.
Cancer Genet Cytogenet, 168(2) 2006, 181-82.
(PMID 16843114)
|
|
| banding: 1 |
Vasquez-Jimenez EA, Romo-Martinez EJ, Meza-Espinoza JP, Lopez-Guido B, et al.
A new complex chromosomal translocation t(2;12;21)(q33;p13;q22) in B-cell acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 168(2) 2006, 179-80.
(PMID 16843113)
|
|
| banding: 1 |
South ST, Frazer JK, Brothman AR, and Chen Z.
Unexpected cytogenetic finding in acute lymphoblastic leukemia: a case of del(5q) with a cryptic t(12;21).
Cancer Genet Cytogenet, 168(2) 2006, 177-78.
(PMID 16843112)
|
|
| banding: 1 |
Wu SQ, Lu G, Chen XR, and Quinn J.
Simultaneous presence of t(10;11)(p12;q23) and t(11;19)(q23;p13.1) in an infantile acute myeloid leukemia.
Cancer Genet Cytogenet, 168(2) 2006, 175-76.
(PMID 16843111)
|
|
| banding: 2 |
Bacher U, Schnittger S, Kern W, Trenn G, Weisser M, Haferlach T, et al.
Acute myeloid leukemia (AML) with t(8;21)(q22;q22) relapsing as AML with t(3;21)(q26;q22).
Cancer Genet Cytogenet, 168(2) 2006, 172-74.
(PMID 16843110)
|
|
| banding: 1 |
Kadkol SS, Bruno A, Oh S, Schmidt ML, and Lindgren V.
MLL-SEPT6 fusion transcript with a novel sequence in an infant with acute myeloid leukemia.
Cancer Genet Cytogenet, 168(2) 2006, 162-67.
(PMID 16843108)
|
|
| banding: 1 |
He M, Das K, Blacksin M, Benevenia J, and Hameed M.
A translocation involving the placental growth factor gene is identified in an epithelioid hemangioendothelioma.
Cancer Genet Cytogenet, 168(2) 2006, 150-54.
(PMID 16843105)
|
|
| banding: 2 |
Stasik C, Ganguly S, Cunningham MT, Hagemeister S, and Persons DL.
Infant acute lymphoblastic leukemia with t(11;16)(q23;p13.3) and lineage switch into acute monoblastic leukemia.
Cancer Genet Cytogenet, 168(2) 2006, 146-49.
(PMID 16843104)
|
|
| banding: 42 |
Shali W, Helias C, Fohrer C, Struski S, Gervais C, Falkenrodt A, Leymarie V, et al.
Cytogenetic studies of a series of 43 consecutive secondary myelodysplastic syndromes/acute myeloid leukemias: conventional cytogenetics, FISH, and multiplex FISH.
Cancer Genet Cytogenet, 168(2) 2006, 133-45.
(PMID 16843103)
|
|
| banding: 35 |
Bang SM, Kim YR, Cho HI, Chi HS, Seo EJ, Park CJ, Yoo SJ, Kim HC, Chun HG, Min HC, et al.
Identification of 13q deletion, trisomy 1q, and IgH rearrangement as the most frequent chromosomal changes found in Korean patients with multiple myeloma.
Cancer Genet Cytogenet, 168(2) 2006, 124-32.
(PMID 16843102)
|
|
| banding: 5 |
Athanasiadou A, Stamatopoulos K, Tsompanakou A, Gaitatzi M, Kalogiannidis P, et al.
Clinical, immunophenotypic, and molecular profiling of trisomy 12 in chronic lymphocytic leukemia and comparison with other karyotypic subgroups defined by cytogenetic . . .
Cancer Genet Cytogenet, 168(2) 2006, 109-19.
(PMID 16843100)
|
|
| banding: 1 |
Rezk S, Wheelock L, Fletcher JA, Oliveira AM, Keuker CP, Newburger PE, Xu B, Woda BA, et al.
Acute lymphocytic leukemia with eosinophilia and unusual karyotype.
Leuk Lymphoma, 47(6) 2006, 1176-79.
(PMID 16840218)
|
|
| banding: 1 |
Rosati R, La Starza R, Luciano L, Gorello P, Matteucci C, Pierini V, Romoli S, et al.
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia.
Leukemia, 20(9) 2006, 1623-24.
(PMID 16838028)
|
|
| banding: 1 |
Cole B, Zhou H, McAllister N, Afify Z, and Coffin CM.
Inflammatory myofibroblastic tumor with thrombocytosis and a unique chromosomal translocation With ALK rearrangement.
Arch Pathol Lab Med, 130(7) 2006, 1042-45.
(PMID 16831032)
|
|
| banding: 1 |
Sagawa M, Shimizu T, Shimizu T, Awaya N, Mitsuhashi T, Ikeda Y, Okamoto S, et al.
Establishment of a new human acute monocytic leukemia cell line TZ-1 with t(1;11)(p32;q23) and fusion gene MLL-EPS15.
Leukemia, 20(9) 2006, 1566-71.
(PMID 16826222)
|
|
| banding: 8 |
Schaad K, Strombeck B, Mandahl N, Andersen MK, Heim S, Mertens F, et al.
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the . . .
Cytogenet Genome Res, 114(2) 2006, 126-30.
(PMID 16825763)
|
|
| CGH: 2
banding: 2 |
Ishiguro M, Iwasaki H, Takeshita M, Hirose Y, and Kaneko Y.
A cytogenetic analysis in two cases of malignant peripheral nerve sheath tumor showing hypodiploid karyotype.
Oncol Rep, 16(2) 2006, 225-32.
(PMID 16820897)
|
|
| banding: 8 |
Calabrese G, Fantasia D, Di Gianfilippo R, Stuppia L, Di Lorenzo R, et al.
Fluorescence in situ hybridization analysis of minimal residual disease and the relevance of the der(9) deletion in imatinib-treated patients with chronic myeloid . . .
Haematologica, 91(7) 2006, 994-95.
(PMID 16818290)
|
|
| banding: 1 |
Suenaga M, Matsushita K, Kawamata N, Kukita T, Hamakawa Y, Gejima K, Onodera R, et al.
True malignant histiocytosis with trisomy 9 following primary mediastinal germ cell tumor.
Acta Haematol, 116(1) 2006, 62-66.
(PMID 16809892)
|
|
| banding: 1 |
Su X, Drabkin H, Clappier E, Morgado E, Busson M, Romana S, Soulier J, Berger R, et al.
Transforming potential of the T-cell acute lymphoblastic leukemia-associated homeobox genes HOXA13, TLX1, and TLX3.
Genes Chromosomes Cancer, 45(9) 2006, 846-55.
(PMID 16804919)
|
|
| banding: 2 |
Quintas-Cardama A, Abruzzo LV, Giles FJ, Jorgensen J, Cortes J, Sarriera JE, et al.
A novel translocation t(3;21)(p21;q22) in acute myelogenous leukemia preceding a late-appearing Philadelphia chromosome.
Leukemia, 20(9) 2006, 1638-40.
(PMID 16791272)
|
|
| aCGH: 10
banding: 10 |
Goldstein M, Meller I, Issakov J, and Orr-Urtreger A.
Novel genes implicated in embryonal, alveolar, and pleomorphic rhabdomyosarcoma: a cytogenetic and molecular analysis of primary tumors.
Neoplasia, 8(5) 2006, 332-43.
(PMID 16790082)
|
|
| banding: 17 |
Georgiou G, Karali V, Zouvelou C, Kyriakou E, Dimou M, Chrisochoou S, Greka P, et al.
Serial determination of FLT3 mutations in myelodysplastic syndrome patients at diagnosis, follow up or acute myeloid leukaemia transformation: incidence and their prognostic . . .
Br J Haematol, 134(3) 2006, 302-06.
(PMID 16787503)
|
|
| banding: 1 |
Wong WS, Cheng KC, Lau KM, Chan NP, Shing MM, Cheng SH, Chik KW, Li CK, et al.
Clonal evolution of 8p11 stem cell syndrome in a 14-year-old Chinese boy: a review of literature of t(8;13) associated myeloproliferative diseases.
Leuk Res, 31(2) 2007, 235-38.
(PMID 16777224)
|
|
| banding: 1 |
Reader JC, Zhao XF, Butler MS, Rapoport AP, and Ning Y.
REL-positive double minute chromosomes in follicular lymphoma.
Leukemia, 20(9) 2006, 1624-26.
(PMID 16775615)
|
|
| banding: 1 |
Buijs A, Terhal PA, and Thunnissen PL.
Philadelphia chromosome of a constitutional der(22)t(Y;22)(q11.2;p11) with a variant t(1;9;22)(p36;q34;q11) in a case of chronic myelogenous leukemia.
Cancer Genet Cytogenet, 168(1) 2006, 80-82.
(PMID 16772126)
|
|
| banding: 1 |
Quigley DI and Wolff DJ.
Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci.
Cancer Genet Cytogenet, 168(1) 2006, 77-79.
(PMID 16772125)
|
|
| banding: 1 |
Garcia-Casado Z, Cervera J, Valencia A, Pajuelo JC, Mena-Duran AV, Barragan E, et al.
A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia.
Cancer Genet Cytogenet, 168(1) 2006, 73-76.
(PMID 16772124)
|
|
| banding: 1 |
Sandlund JT, Kastan MB, Kennedy W, Behm F, Entrekin E, Pui CH, Kalwinsky DT, et al.
A subtle t(3;8) results in plausible juxtaposition of MYC and BCL6 in a child with Burkitt lymphoma/leukemia and ataxia-telangiectasia.
Cancer Genet Cytogenet, 168(1) 2006, 69-72.
(PMID 16772123)
|
|
| banding: 17 |
Phan TX, Hoang AV, Huynh VM, Nguyen KT, Nguyen TB, Huynh N, Pham QT, Tran VB, Tran VB, et al.
Unique secondary chromosomal abnormalities are frequently found in the chronic phase of chronic myeloid leukemia in southern Vietnam.
Cancer Genet Cytogenet, 168(1) 2006, 59-68.
(PMID 16772122)
|
|
| banding: 1 |
McGhee EM, Cotter PD, Weier JF, Berline JW, Turner MA, Gormley M, et al.
Molecular cytogenetic characterization of human papillomavirus16-transformed foreskin keratinocyte cell line 16-MT.
Cancer Genet Cytogenet, 168(1) 2006, 36-43.
(PMID 16772119)
|
|
| banding: 16 |
Babicka L, Zemanova Z, Pavlistova L, Brezinova J, Ransdorfova S, Houskova L, et al.
Complex chromosomal rearrangements in patients with chronic myeloid leukemia.
Cancer Genet Cytogenet, 168(1) 2006, 22-29.
(PMID 16772117)
|
|
| banding: 1 |
Hayne CC, Winer E, Williams T, Chaves F, Khorsand J, and Mark HF.
Acute lymphoblastic leukemia with 4;11 translocation analyzed by a multi-modal strategy of conventional cytogenetics, FISH, morphology, flow cytometry and molecular genetics, and review of . . .
Exp Mol Pathol, 81(1) 2006, 62-71.
(PMID 16765346)
|
|
| banding: 1 |
Janssen H, Wlodarska I, Mecucci C, Hagemeijer A, Vandenberghe P, Marynen P, et al.
Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).
Haematologica, 91(7) 2006, 949-51.
(PMID 16757412)
|
|
| banding: 1 |
Nakaya A, Ogihara T, and Awaya N.
Plasma cell leukemia presenting with diplopia due to unilateral abducens paralysis and complex chromosomal abnormalities.
Intern Med, 45(9) 2006, 637-40.
(PMID 16755096)
|
|
| banding: 15 |
Mahmoud LA, Shamaa SS, Salem MA, Aladle DA, and Goda EF.
A study for evaluation of different diagnostic approaches in acute leukemia in Egypt.
Hematology, 11(2) 2006, 87-95.
(PMID 16753847)
|
|
| banding: 1 |
Al-Quran SZ, Olivares A, Lin P, Stephens TW, Medeiros LJ, and Abruzzo LV.
Myeloid sarcoma of the urinary bladder and epididymis as a primary manifestation of acute myeloid leukemia with inv(16).
Arch Pathol Lab Med, 130(6) 2006, 862-66.
(PMID 16740041)
|
|
| banding: 1 |
Haimi M, Avivi I, Moustafa N, Aboleil O, and Gershoni-Baruch R.
Treatment-related acute myeloid leukemia characterized by t(11;20)(p15;q11) and del(9)(q22).
Cancer Genet Cytogenet, 167(2) 2006, 186-88.
(PMID 16737924)
|
|
| banding: 1 |
Gozzetti A, Crupi R, Tozzuoli D, Calabrese S, Bocchia M, Pirrotta MT, Raspadori D, et al.
Trisomy 13 in a patient with acute myeloid leukemia M0 and unusual durable remission.
Cancer Genet Cytogenet, 167(2) 2006, 182.
(PMID 16737922)
|
|
| banding: 13 |
Fink SR, Smoley SA, Stockero KJ, Paternoster SF, Thorland EC, Van Dyke DL, et al.
Loss of TP53 is due to rearrangements involving chromosome region 17p10 approximately p12 in chronic lymphocytic leukemia.
Cancer Genet Cytogenet, 167(2) 2006, 177-81.
(PMID 16737921)
|
|
| banding: 1 |
Choi HW, Shin MG, Sawyer JR, Cho D, Kee SJ, Baek HJ, Kook H, Kim HJ, Shin JH, Suh SP, et al.
Unusual type of TLS/FUS-ERG chimeric transcript in a pediatric acute myelocytic leukemia with 47,XX,+10,t(16;21)(p11;q22).
Cancer Genet Cytogenet, 167(2) 2006, 172-76.
(PMID 16737920)
|
|
| banding: 1 |
Yoo SJ, Seo EJ, Lee JH, Seo YH, Park PW, and Ahn JY.
A complex, four-way variant t(15;17) in acute promyelocytic leukemia.
Cancer Genet Cytogenet, 167(2) 2006, 168-71.
(PMID 16737919)
|
|
| banding: 2 |
Pedrazzini E, Cerretini R, Noriega MF, Narbaitz M, Palacios MF, Negri P, Bengio R, et al.
Inversions of chromosomes 2 and 6 in mantle cell lymphoma. Cytogenetic, FISH, and molecular studies.
Cancer Genet Cytogenet, 167(2) 2006, 164-67.
(PMID 16737918)
|
|
| banding: 1 |
Shetty S, Mansoor A, and Roland B.
Ring chromosome 7 with amplification of 7q sequences in a pediatric case of hepatosplenic T-cell lymphoma.
Cancer Genet Cytogenet, 167(2) 2006, 161-63.
(PMID 16737917)
|
|
| banding: 1 |
Pawarode A, Finlay E, Sait SN, Barcos M, and Baer MR.
Isochromosome 1q in a myelodysplastic syndrome after treatment for acute promyelocytic leukemia.
Cancer Genet Cytogenet, 167(2) 2006, 155-60.
(PMID 16737916)
|
|
| banding: 17 |
Ishii Y, Hsiao HH, Sashida G, Ito Y, Miyazawa K, Kodama A, Ohyashiki JH, et al.
Derivative (1;7)(q10;p10) in multiple myeloma. A sign of therapy-related hidden myelodysplastic syndrome.
Cancer Genet Cytogenet, 167(2) 2006, 131-37.
(PMID 16737912)
|
|
| CGH: 11
banding: 11 |
Uchida K, Oga A, Okafuji M, Mihara M, Kawauchi S, Furuya T, Chochi Y, Ueyama Y, et al.
Molecular cytogenetic analysis of oral squamous cell carcinomas by comparative genomic hybridization, spectral karyotyping, and fluorescence in situ hybridization.
Cancer Genet Cytogenet, 167(2) 2006, 109-16.
(PMID 16737909)
|
|
| banding: 1 |
Zagaria A, Anelli L, Albano F, Vicari L, Schiavone EM, Annunziata M, Pane F, Liso V, et al.
Molecular cytogenetic characterization of deletions on der(9) in chronic myelocytic leukemia.
Cancer Genet Cytogenet, 167(2) 2006, 97-102.
(PMID 16737907)
|
|
| banding: 31 |
Zatkova A, Schoch C, Speleman F, Poppe B, Mannhalter C, Fonatsch C, et al.
GAB2 is a novel target of 11q amplification in AML/MDS.
Genes Chromosomes Cancer, 45(9) 2006, 798-807.
(PMID 16736498)
|
|
| banding: 11 |
Sawyer JR, Husain M, and Al-Mefty O.
Identification of isochromosome 1q as a recurring chromosome aberration in skull base chordomas: a new marker for aggressive tumors?
Neurosurg Focus, 10(3) 2001, E6.
(PMID 16734409)
|
|
| banding: 2 |
Panani AD.
Cytogenetic findings in untreated patients with essential thrombocythemia.
In Vivo, 20(3) 2006, 381-84.
(PMID 16724675)
|
|
| banding: 1 |
Panani AD.
Gain of an isochromosome 5p: a rare recurrent abnormality in acute myeloid leukemia.
In Vivo, 20(3) 2006, 359-60.
(PMID 16724670)
|
|
| banding: 17 |
Storlazzi CT, Brekke HR, Mandahl N, Brosjo O, Smeland S, Lothe RA, et al.
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours.
J Pathol, 209(4) 2006, 492-500.
(PMID 16721726)
|
|
| CGH: 17
aCGH: 17
banding: 17 |
Rucker FG, Sander S, Dohner K, Dohner H, Pollack JR, and Bullinger L.
Molecular profiling reveals myeloid leukemia cell lines to be faithful model systems characterized by distinct genomic aberrations.
Leukemia, 20(6) 2006, 994-1001.
(PMID 16721385)
|
|
| banding: 2 |
Takei N, Suzukawa K, Mukai HY, Itoh T, Okoshi Y, Yoda Y, and Nagasawa T.
Therapy-related acute myeloid leukemia 6 years after clonal detection of inv(11)(q21q23) and MLL gene rearrangement.
Int J Hematol, 83(3) 2006, 247-51.
(PMID 16720556)
|
|
| banding: 1 |
Sumi M, Nunoda K, Mizutani T, Ishii Y, Gotoh A, Kimura Y, Suga Y, Ohira T, et al.
Hypereosinophilia in a patient with invasive thymoma with clonal T-lymphocyte expansion expressing CD4, CD8, and CD25 antigens.
Int J Hematol, 83(3) 2006, 243-46.
(PMID 16720555)
|
|
| banding: 2 |
Kawamura-Saito M, Yamazaki Y, Kaneko K, Kawaguchi N, Kanda H, Mukai H, Gotoh T, et al.
Fusion between CIC and DUX4 up-regulates PEA3 family genes in Ewing-like sarcomas with t(4;19)(q35;q13) translocation.
Hum Mol Genet, 15(13) 2006, 2125-37.
(PMID 16717057)
|
|
| banding: 1 |
Wang TF, Horsley SW, Lee KF, Chu SC, Li CC, and Kao RH.
Translocation between chromosome 5q35 and chromosome 11q13-- an unusual cytogenetic finding in a primary refractory acute myeloid leukemia.
Clin Lab Haematol, 28(3) 2006, 160-63.
(PMID 16706931)
|
|
| CGH: 9
aCGH: 10
banding: 13 |
Strefford JC, van Delft FW, Robinson HM, Worley H, Yiannikouris O, Selzer R, et al.
Complex genomic alterations and gene expression in acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21.
Proc Natl Acad Sci U S A, 103(21) 2006, 8167-72.
(PMID 16702559)
|
|
| banding: 1 |
Burmeister T, Macleod RA, Reinhardt R, Mansmann V, Loddenkemper C, Marinets O, et al.
A novel sporadic Burkitt lymphoma cell line (BLUE-1) with a unique t(6;20)(q15;q11.2) rearrangement.
Leuk Res, 30(11) 2006, 1417-23.
(PMID 16697040)
|
|
| banding: 1 |
Chevret E, Prochazkova M, Beylot-Barry M, and Merlio JP.
A suggested protocol for obtaining high-quality skin metaphases from primary cutaneous T-cell lymphoma.
Cancer Genet Cytogenet, 167(1) 2006, 89-91.
(PMID 16682294)
|
|
| banding: 1 |
Roberts KA, Martineau M, Broadfield ZJ, Gibson BE, Harewood L, Stewart J, et al.
A diminutive chromosome 21 centromere in acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 167(1) 2006, 78-81.
(PMID 16682292)
|
|
| banding: 1 |
Oliver JW, Farnsworth B, and Tonk VS.
Juvenile myelomonocytic leukemia in a child with Crohn disease.
Cancer Genet Cytogenet, 167(1) 2006, 70-73.
(PMID 16682290)
|
|
| banding: 13 |
Royer-Pokora B, Trost D, Muller N, Hildebrandt B, Germing U, et al.
Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia.
Cancer Genet Cytogenet, 167(1) 2006, 66-69.
(PMID 16682289)
|
|
| banding: 3 |
Olshanskaya YV, Udovichenko AI, Vodinskaya LA, Glasko EN, Parovitchnikova EN, et al.
Myelodysplastic syndromes with isolated deletion of the long arm of the chromosome X as a sole cytogenetic change.
Cancer Genet Cytogenet, 167(1) 2006, 47-50.
(PMID 16682286)
|
|
| banding: 1 |
Murphy PT, Mitra S, and ODonghaile D.
Another case of myelodysplasia with monosomy 7 following fludarabine-based chemotherapy.
Am J Hematol, 81(6) 2006, 473.
(PMID 16680754)
|
|
| banding: 1 |
Lazarevic V, Golovleva I, Nygren I, and Wahlin A.
Induction chemotherapy and post-remission imatinib therapy for de Novo BCR-ABL-positive AML.
Am J Hematol, 81(6) 2006, 470-71.
(PMID 16680752)
|
|
| banding: 1 |
Jelic TM, Berry PK, Jubelirer SJ, Plumley L, Hartel PH, Estalilla OC, et al.
Primary cutaneous follicle center lymphoma of the arm with a novel chromosomal translocation t(12;21)(q13;q22): a case report.
Am J Hematol, 81(6) 2006, 448-53.
(PMID 16680749)
|
|
| banding: 4 |
Au WY, Chan LC, Liang R, and Kwong YL.
Myelodysplastic syndrome and acute myeloid leukemia after treatment with fludarabine, mitoxantrone, and dexamethasone.
Am J Hematol, 81(6) 2006, 471-73.
(PMID 16680740)
|
|
| banding: 1 |
Leong CF, Azma RZ, Cheong SK, Salwati S, and Sharifah NA.
Complex karyotypic abnormalities in a case of acute myeloid leukaemia--M4Eo.
Malays J Pathol, 27(1) 2005, 45-50.
(PMID 16676693)
|
|
| banding: 26 |
Cauwelier B, Dastugue N, Cools J, Poppe B, Herens C, De Paepe A, Hagemeijer A, et al.
Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCRbeta locus rearrangements and putative new T-cell oncogenes.
Leukemia, 20(7) 2006, 1238-44.
(PMID 16673021)
|
|
| banding: 5 |
von Bergh AR, van Drunen E, van Wering ER, van Zutven LJ, Hainmann I, Lonnerholm G, et al.
High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9.
Genes Chromosomes Cancer, 45(8) 2006, 731-39.
(PMID 16646086)
|
|
| banding: 1 |
Panagopoulos I, Strombeck B, Isaksson M, Heldrup J, Olofsson T, et al.
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.
Br J Haematol, 133(3) 2006, 270-75.
(PMID 16643428)
|
|
| banding: 1 |
Bigby SM, Oei P, Lambie NK, and Symmans PJ.
Dermatofibrosarcoma protuberans: report of a case with a variant ring chromosome and metastases following pregnancy.
J Cutan Pathol, 33(5) 2006, 383-88.
(PMID 16640548)
|
|
| banding: 1 |
Pinheiro RF, Chauffaille Mde L, and Silva MR.
Isochromosome 17q in MDS: a marker of a distinct entity.
Cancer Genet Cytogenet, 166(2)(2) 2006, 189-90.
(PMID 16631479)
|
|
| banding: 1 |
Manor E, Sion-Vardy N, and Bodner L.
Cytogenetic and fluorescence in situ hybridization analysis of a basal cell adenocarcinoma of the mandible.
Cancer Genet Cytogenet, 166(2) 2006, 186-88.
(PMID 16631478)
|
|
| banding: 1 |
Todoric-Zivanovic B, Marisavljevic D, Surace C, Cemerikic V, Markovic O, Krtolica K, et al.
A Ph-negative chronic myeloid leukemia with a complex BCR/ABL rearrangement and a t(6;9)(p21;q34.1).
Cancer Genet Cytogenet, 166(2) 2006, 180-85.
(PMID 16631477)
|
|
| banding: 1 |
Castryck H, van den Driessche M, Hagemeijer A, Stul M, Wynendaele W, Vandenberghe P, et al.
Coexistence of light chain disease and chronic lymphocytic leukaemia, a complex karyotype with a rapid fatal outcome.
Clin Lab Haematol, 28(2) 2006, 138-40.
(PMID 16630221)
|
|
| banding: 2 |
Streubel B, Scheucher B, Valencak J, Huber D, Petzelbauer P, Trautinger F, et al.
Molecular cytogenetic evidence of t(14;18)(IGH;BCL2) in a substantial proportion of primary cutaneous follicle center lymphomas.
Am J Surg Pathol, 30(4) 2006, 529-36.
(PMID 16625101)
|
|
| banding: 17 |
Marzin Y, Jamet D, Douet-Guilbert N, Morel F, Le Bris MJ, Morice P, Abgrall JF, et al.
Chromosome 1 abnormalities in multiple myeloma.
Anticancer Res, 26(2A) 2006, 953-59.
(PMID 16619492)
|
|
| banding: 6 |
Trubia M, Albano F, Cavazzini F, Cambrin GR, Quarta G, Fabbiano F, Ciambelli F, et al.
Characterization of a recurrent translocation t(2;3)(p15-22;q26) occurring in acute myeloid leukaemia.
Leukemia, 20(1) 2006, 48-54.
(PMID 16619048)
|
|
| banding: 34 |
Ruminy P, Jardin F, Picquenot JM, Gaulard P, Parmentier F, Buchonnet G, et al.
Two patterns of chromosomal breakpoint locations on the immunoglobulin heavy-chain locus in B-cell lymphomas with t(3;14)(q27;q32): relevance to histology.
Oncogene, 25(35) 2006, 4947-54.
(PMID 16619046)
|
|
| CGH: 2
aCGH: 1
banding: 18 |
La Starza R, Aventin A, Matteucci C, Crescenzi B, Romoli S, Testoni N, Pierini V, et al.
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia.
Leukemia, 20(6) 2006, 958-64.
(PMID 16617324)
|
|
| banding: 8 |
Costa D, Carrio A, Madrigal I, Arias A, Valera A, Colomer D, Aguilar JL, Teixido M, et al.
Studies of complex Ph translocations in cases with chronic myelogenous leukemia and one with acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 166(1) 2006, 89-93.
(PMID 16616117)
|
|
| banding: 3 |
Smith A, Das P, OReilly J, Patsouris C, and Campbell LJ.
Three adults with acute lymphoblastic leukemia and dic(7;9)(p11.2;p11).
Cancer Genet Cytogenet, 166(1) 2006, 86-88.
(PMID 16616116)
|
|
| banding: 5 |
Lin P, Medeiros LJ, Yin CC, and Abruzzo LV.
Translocation (3;8)(q26;q24): a recurrent chromosomal abnormality in myelodysplastic syndrome and acute myeloid leukemia.
Cancer Genet Cytogenet, 166(1) 2006, 82-85.
(PMID 16616115)
|
|
| CGH: 5
aCGH: 5
banding: 5 |
Park SJ, Jeong SY, and Kim HJ.
Y chromosome loss and other genomic alterations in hepatocellular carcinoma cell lines analyzed by CGH and CGH array.
Cancer Genet Cytogenet, 166(1) 2006, 56-64.
(PMID 16616112)
|
|
| banding: 18 |
Hassler M, Seidl S, Fazeny-Doerner B, Preusser M, Hainfellner J, Rossler K, Prayer D, et al.
Diversity of cytogenetic and pathohistologic profiles in glioblastoma.
Cancer Genet Cytogenet, 166(1) 2006, 46-55.
(PMID 16616111)
|
|
| banding: 2 |
Reddy K, Satyadev R, Bouman D, Hibbard MK, Lu G, and Paolo R.
Burkitt t(8;14)(q24;q32) and cryptic deletion in a CLL patient: report of a case and review of literature.
Cancer Genet Cytogenet, 166(1) 2006, 12-21.
(PMID 16616107)
|
|
| banding: 104 |
Jeandidier E, Dastugue N, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, et al.
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique . . .
Cancer Genet Cytogenet, 166(1) 2006, 1-11.
(PMID 16616106)
|
|
| banding: 1 |
Braham Jmili N, Omri H, Senana Sendi H, Fekih S, Hizem S, Sriha B, Khelif A, Saad A, et al.
Identification of the translocation t(15;17) in acute myeloid leukemia (AML) initially classified as FAB M1: case report and review of the literature.
Clin Lab, 52(3-4) 2006, 125-30.
(PMID 16584058)
|
|
| banding: 8 |
Torlakovic EE, Aamot HV, and Heim S.
A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma.
J Pathol, 209(2) 2006, 258-64.
(PMID 16583359)
|
|
| banding: 10 |
Kirschnerova G, Tothova A, and Babusikova O.
Amplification of AML1 gene in association with karyotype, age and diagnosis in acute leukemia patients.
Neoplasma, 53(2) 2006, 150-54.
(PMID 16575471)
|
|
| banding: 103 |
Bao L, Wang X, Ryder J, Ji M, Chen Y, Chen H, Sun H, Yang Y, Du X, Kerzic P, Gross SA, et al.
Prospective study of 174 de novo acute myelogenous leukemias according to the WHO classification: subtypes, cytogenetic features and FLT3 mutations.
Eur J Haematol, 77(1) 2006, 35-45.
(PMID 16573742)
|
|
| banding: 15 |
Auewarakul CU, Lauhakirti D, and Tocharoentanaphol C.
Frequency of RAS gene mutation and its cooperative genetic events in Southeast Asian adult acute myeloid leukemia.
Eur J Haematol, 77(1) 2006, 51-56.
(PMID 16573741)
|
|
| banding: 6 |
Gil Z, Orr-Urtreger A, Voskoboinik N, Trejo-Leider L, Spektor S, Shomrat R, et al.
Cytogenetic analysis of sinonasal carcinomas.
Otolaryngol Head Neck Surg, 134(4) 2006, 654-60.
(PMID 16564392)
|
|
| banding: 1 |
Cogulu O, Karapinar DY, Karaca E, Aydinok Y, and Ozkinay F.
Unusual course of an acute lymphoblastic leukemia case with i(9q) as a sole cytogenetic abnormality.
Leuk Res, 30(11) 2006, 1461-63.
(PMID 16564090)
|
|
| banding: 1 |
Choo PH, Arain SA, Carolan JA, Roth AM, and West DC.
Extramedullary myeloid leukemia: the value of cytogenetic analysis in pediatric orbital tumors.
Ophthal Plast Reconstr Surg, 22(2) 2006, 143-45.
(PMID 16550066)
|
|
| banding: 1 |
Carneiro BA, Kaminer L, Eldibany M, Sreekantaiah C, Kaul K, and Locker GY.
Oxaliplatin-related acute myelogenous leukemia.
Oncologist, 11(3) 2006, 261-62.
(PMID 16549810)
|
|
| banding: 2 |
Karrman K, Andersson A, Bjorgvinsdottir H, Strombeck B, Lassen C, Olofsson T, et al.
Deregulation of cyclin D2 by juxtaposition with T-cell receptor alpha/delta locus in t(12;14)(p13;q11)-positive childhood T-cell acute lymphoblastic leukemia.
Eur J Haematol, 77(1) 2006, 27-34.
(PMID 16548914)
|
|
| banding: 1 |
Pelosini M, Benedetti E, Galimberti S, Caracciolo F, Petrini M, Fazzi R, et al.
Granulocytic sarcoma and subsequent acute leukemia recurrence with different biologic characteristics 5 years after allogeneic bone marrow transplantation for acute myeloid . . .
Bone Marrow Transplant, 37(9) 2006, 897-98.
(PMID 16547489)
|
|
| banding: 1 |
Sharif K, Ramani P, Lochbuhler H, Grundy R, and de Ville de Goyet J.
Recurrent mesenchymal hamartoma associated with 19q translocation. A call for more radical surgical resection.
Eur J Pediatr Surg, 16(1) 2006, 64-67.
(PMID 16544232)
|
|
| banding: 1 |
Engleson J, Soller M, Panagopoulos I, Dahlen A, Dictor M, and Jerkeman M.
Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy.
BMC Cancer, 6 2006, 69.
(PMID 16542442)
|
|
| banding: 1 |
Alaggio R, Ninfo V, Rosolen A, and Coffin CM.
Primitive myxoid mesenchymal tumor of infancy: a clinicopathologic report of 6 cases.
Am J Surg Pathol, 30(3) 2006, 388-94.
(PMID 16538060)
|
|
| banding: 3 |
Yamamoto T, Isomura M, Xu Y, Liang J, Yagasaki H, Kamachi Y, Kudo K, Kiyoi H, Naoe T, et al.
PTPN11, RAS and FLT3 mutations in childhood acute lymphoblastic leukemia.
Leuk Res, 30(9) 2006, 1085-89.
(PMID 16533526)
|
|
| banding: 26 |
Yin CC, Cortes J, Barkoh B, Hayes K, Kantarjian H, and Jones D.
t(3;21)(q26;q22) in myeloid leukemia: an aggressive syndrome of blast transformation associated with hydroxyurea or antimetabolite therapy.
Cancer, 106(8) 2006, 1730-38.
(PMID 16532439)
|
|
| banding: 3 |
Yeung J, Kempski H, Neat M, Bailey S, Smith O, and Brady HJ.
Characterization of the t(17;19) translocation by gene-specific fluorescent in situ hybridization-based cytogenetics and detection of the E2A-HLF fusion transcript and protein in patients . . .
Haematologica, 91(3) 2006, 422-24.
(PMID 16531271)
|
|
| banding: 1 |
Tchinda J, Volpert S, Berdel WE, Buchner T, and Horst J.
Novel three-break rearrangement and cryptic translocations leading to colocalization of MYC and IGH signals in B-cell acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 165(2) 2006, 180-84.
(PMID 16527615)
|
|
| banding: 1 |
Aamot HV, Tjonnfjord GE, Delabie J, and Heim S.
Molecular cytogenetic analysis of leukemic mantle cell lymphoma with a cryptic t(11;14).
Cancer Genet Cytogenet, 165(2) 2006, 172-75.
(PMID 16527613)
|
|
| banding: 23 |
Hsiao HH, Sashida G, Ito Y, Kodama A, Fukutake K, Ohyashiki JH, et al.
Additional cytogenetic changes and previous genotoxic exposure predict unfavorable prognosis in myelodysplastic syndromes and acute myeloid leukemia with der(1;7)(q10;p10).
Cancer Genet Cytogenet, 165(2) 2006, 161-66.
(PMID 16527611)
|
|
| banding: 1 |
Qian YW, Malliah R, Lee HJ, Das K, Mirani N, and Hameed M.
A t(12;17) in an extraorbital giant cell angiofibroma.
Cancer Genet Cytogenet, 165(2) 2006, 157-60.
(PMID 16527610)
|
|
| banding: 17 |
Vidarsson H, Steinarsdottir M, Jonasson JG, Juliusdottir H, Hauksdottir H, et al.
Effect of hypoxia and TP53 mutation status and cytogenetics of normal and malignant mammary epithelium.
Cancer Genet Cytogenet, 165(2) 2006, 144-50.
(PMID 16527608)
|
|
| banding: 20 |
Taborelli M, Tibiletti MG, Martin V, Pozzi B, Bertoni F, and Capella C.
Chromosome band 6q deletion pattern in malignant lymphomas.
Cancer Genet Cytogenet, 165(2) 2006, 106-13.
(PMID 16527604)
|
|
| banding: 7 |
Kobayashi C, Oda Y, Takahira T, Izumi T, Kawaguchi K, Yamamoto H, Tamiya S, Yamada T, et al.
Chromosomal aberrations and microsatellite instability of malignant peripheral nerve sheath tumors: a study of 10 tumors from nine patients.
Cancer Genet Cytogenet, 165(2) 2006, 98-105.
(PMID 16527603)
|
|
| banding: 20 |
Karst C, Gross M, Haase D, Wedding U, Hoffken K, Liehr T, and Mkrtchyan H.
Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
Int J Oncol, 28(4) 2006, 891-97.
(PMID 16525638)
|
|
| banding: 33 |
Farag SS, Archer KJ, Mrozek K, Ruppert AS, Carroll AJ, Vardiman JW, Pettenati MJ, et al.
Pretreatment cytogenetics add to other prognostic factors predicting complete remission and long-term outcome in patients 60 years of age or older with acute myeloid leukemia: results from . . .
Blood, 108(1) 2006, 63-73.
(PMID 16522815)
|
|
| banding: 30 |
Cerretini R, Noriega MF, Narbaitz M, and Slavutsky I.
New chromosome abnormalities and lack of BCL-6 gene rearrangements in Argentinean diffuse large B-cell lymphomas.
Eur J Haematol, 76(4) 2006, 284-93.
(PMID 16519699)
|
|
| banding: 1 |
Sindt A, Deau B, Brahim W, Staal A, Visanica S, Villarese P, Rault JP, Macintyre E, et al.
Acute monocytic leukemia with coexpression of minor BCR-ABL1 and PICALM-MLLT10 fusion genes along with overexpression of HOXA9.
Genes Chromosomes Cancer, 45(6) 2006, 575-82.
(PMID 16518848)
|
|
| CGH: 34
banding: 23 |
Watanabe N, Nakadate H, Haruta M, Sugawara W, Sasaki F, Tsunematsu Y, Kikuta A, et al.
Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor.
Genes Chromosomes Cancer, 45(6) 2006, 592-601.
(PMID 16518847)
|
|
| banding: 1 |
Granville L, Hicks J, Popek E, Dishop M, Tatevian N, and Lopez-Terrada D.
Visceral clear cell sarcoma of soft tissue with confirmation by EWS-ATF1 fusion detection.
Ultrastruct Pathol, 30(1) 2006, 111-18.
(PMID 16517477)
|
|
| banding: 1 |
Holla P, Hafez GR, Slukvin I, and Kalayoglu M.
Synovial sarcoma, a primary liver tumor--a case report.
Pathol Res Pract, 202(5) 2006, 385-87.
(PMID 16503097)
|
|
| banding: 13 |
Paulsson K, Heidenblad M, Strombeck B, Staaf J, Jonsson G, Borg A, Fioretos T, et al.
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic . . .
Leukemia, 20(5) 2006, 840-46.
(PMID 16498392)
|
|
| banding: 1 |
Score J, Curtis C, Waghorn K, Stalder M, Jotterand M, Grand FH, et al.
Identification of a novel imatinib responsive KIF5B-PDGFRA fusion gene following screening for PDGFRA overexpression in patients with hypereosinophilia.
Leukemia, 20(5) 2006, 827-32.
(PMID 16498388)
|
|
| banding: 1 |
Davidsson J, Paulsson K, and Johansson B.
Searching for cryptic chromosomal aberrations in high hyperdiploid childhood acute lymphoblastic leukaemias.
Eur J Haematol, 76(5) 2006, 449-50.
(PMID 16494620)
|
|
| banding: 1 |
Reichard KK, Zhang QY, Sanchez L, Hozier J, Viswanatha D, and Foucar K.
Acute myeloid leukemia of donor origin after allogeneic bone marrow transplantation for precursor T-cell acute lymphoblastic leukemia: case report and review of the . . .
Am J Hematol, 81(3) 2006, 178-85.
(PMID 16493618)
|
|
| banding: 1 |
Lazarevic V, Andersson C, Wahlin A, and Golovleva I.
Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid . . .
Cancer Genet Cytogenet, 165(1) 2006, 87-89.
(PMID 16490605)
|
|
| banding: 1 |
Liu YC, Sashida G, Kodama A, and Ohyashiki K.
Translocation (4;9)(q11;q33), a new rearrangement in acute myeloid leukemia with central nervous system involvement.
Cancer Genet Cytogenet, 165(1) 2006, 85-86.
(PMID 16490604)
|
|
| banding: 1 |
Wong KF, Wong ML, and Tu SP.
Dup(1)(p31.2p36.2) in acute myelomonocytic leukemia.
Cancer Genet Cytogenet, 165(1) 2006, 83-84.
(PMID 16490603)
|
|
| banding: 1 |
de Oliveira FM, Scrideli CA, Queiroz RG, and Tone LG.
Acute lymphoblastic leukemia with inv(5)(q13q31) in a pediatric patient.
Cancer Genet Cytogenet, 165(1) 2006, 81-82.
(PMID 16490602)
|
|
| banding: 1 |
Berger R, Busson M, and Romana SP.
A cryptic chromosome 19 abnormality in a patient with Ph-positive acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 165(1)(1) 2006, 79-80.
(PMID 16490601)
|
|
| banding: 1 |
Mo J, Lampkin B, Perentesis J, Poole L, and Bao L.
Translocation (8;18;16)(p11;q21;p13). A new variant of t(8;16)(p11;p13) in acute monoblastic leukemia: case report and review of the literature.
Cancer Genet Cytogenet, 165(1) 2006, 75-78.
(PMID 16490600)
|
|
| banding: 1 |
Han JY and Theil KS.
The Philadelphia chromosome as a secondary abnormality in inv(3)(q21q26) acute myeloid leukemia at diagnosis: confirmation of p190 BCR-ABL mRNA by real-time quantitative polymerase chain . . .
Cancer Genet Cytogenet, 165(1) 2006, 70-74.
(PMID 16490599)
|
|
| banding: 2 |
Reid AG, Seppa L, von der Weid N, Niggli FK, and Betts DR.
A t(12;17)(p13;q12) identifies a distinct TEL rearrangement-negative subtype of precursor-B acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 165(1) 2006, 64-69.
(PMID 16490598)
|
|
| banding: 20 |
Trost D, Hildebrandt B, Beier M, Muller N, Germing U, and Royer-Pokora B.
Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.
Cancer Genet Cytogenet, 165(1) 2006, 51-63.
(PMID 16490597)
|
|
| banding: 1 |
Gough SM, Benjes SM, McDonald M, Heaton D, Ganly P, and Morris CM.
Translocation (5;10)(q22;q24) in a case of acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 165(1) 2006, 36-40.
(PMID 16490595)
|
|
| banding: 55 |
Preiss BS, Kerndrup GB, Pedersen RK, Hasle H, and Pallisgaard N.
Contribution of multiparameter genetic analysis to the detection of genetic alterations in hematologic neoplasia. An evaluation of combining G-band analysis, spectral karyotyping, and . . .
Cancer Genet Cytogenet, 165(1) 2006, 1-8.
(PMID 16490591)
|
|
| banding: 41 |
Reddy KS.
Chronic lymphocytic leukaemia profiled for prognosis using a fluorescence in situ hybridisation panel.
Br J Haematol, 132(6) 2006, 705-22.
(PMID 16487171)
|
|
| banding: 8 |
Han X, Medeiros LJ, Abruzzo LV, Jones D, and Lin P.
Chronic myeloproliferative diseases with the t(5;12)(q33;p13): clonal evolution is associated with blast crisis.
Am J Clin Pathol, 125(1) 2006, 49-56.
(PMID 16482991)
|
|
| banding: 12 |
Massey GV, Zipursky A, Chang MN, Doyle JJ, Nasim S, Taub JW, Ravindranath Y, Dahl G, et al.
A prospective study of the natural history of transient leukemia (TL) in neonates with Down syndrome (DS): Childrens Oncology Group (COG) study POG-9481.
Blood, 107(12) 2006, 4606-13.
(PMID 16469874)
|
|
| banding: 2 |
Turhan N, Yurur-Kutlay N, Topcuoglu P, Sayki M, Yuksel M, Gurman G, et al.
Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4.
Leuk Res, 30(7) 2006, 903-05.
(PMID 16469377)
|
|
| banding: 23 |
Romana SP, Radford-Weiss I, Ben Abdelali R, Schluth C, Petit A, Dastugue N, et al.
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogenetique Hematologique.
Leukemia, 20(4) 2006, 696-706.
(PMID 16467868)
|
|
| banding: 1 |
Khandelwal A, Seilstad KH, and Magro CM.
Subclinical chronic lymphocytic leukaemia associated with a 13q deletion presenting initially in the skin: apropos of a case.
J Cutan Pathol, 33(3) 2006, 256-59.
(PMID 16466516)
|
|
| CGH: 10
banding: 10 |
Karpova MB, Schoumans J, Blennow E, Ernberg I, Henter JI, Smirnov AF, Nordenskjold M, et al.
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitts lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal . . .
Int J Oncol, 28(3) 2006, 605-17.
(PMID 16465364)
|
|
| banding: 5 |
Daskalakis M, Mauritzson N, Johansson B, Bouabdallah K, Onida F, Kunzmann R, et al.
Trisomy 19 as the sole chromosomal abnormality in proliferative chronic myelomonocytic leukemia.
Leuk Res, 30(8) 2006, 1043-47.
(PMID 16464494)
|
|
| banding: 1 |
Haimi M, Elhasid R, Gershoni-Baruch R, Izraeli S, Wanders RJ, et al.
Myeloid dysplasia in familial 3-methylglutaconic aciduria.
J Pediatr Hematol Oncol, 28(2) 2006, 69-72.
(PMID 16462576)
|
|
| banding: 1 |
Vieira L, Sousa AC, Matos P, Marques B, Alaiz H, Ribeiro MJ, Braga P, da Silva MG, et al.
Three-way translocation involves MLL, MLLT3, and a novel cell cycle control gene, FLJ10374, in the pathogenesis of acute myeloid leukemia with t(9;11;19)(p22;q23;p13.3).
Genes Chromosomes Cancer, 45(5) 2006, 455-69.
(PMID 16450356)
|
|
| banding: 5 |
Behboudi A, Enlund F, Winnes M, Andren Y, Nordkvist A, Leivo I, Flaberg E, Szekely L, et al.
Molecular classification of mucoepidermoid carcinomas-prognostic significance of the MECT1-MAML2 fusion oncogene.
Genes Chromosomes Cancer, 45(5) 2006, 470-81.
(PMID 16444749)
|
|
| banding: 1 |
Kim M, Lim J, Kim Y, Han K, Kang CS, Kim HJ, and Min WS.
A case of therapy-related acute myeloid leukemia associated with inv(16), with subsequent development of t(9;22).
Leukemia, 20(4) 2006, 746-48.
(PMID 16437154)
|
|
| banding: 25 |
Bene MC, Castoldi G, Derolf A, Garand R, Haas T, Haferlach T, Knapp W, Kuhlein E, et al.
Near-tetraploid acute myeloid leukemias: an EGIL retrospective study of 25 cases.
Leukemia, 20(4)(4) 2006, 725-28.
(PMID 16437146)
|
|
| banding: 15 |
Owaidah TM, Al Beihany A, Iqbal MA, Elkum N, and Roberts GT.
Cytogenetics, molecular and ultrastructural characteristics of biphenotypic acute leukemia identified by the EGIL scoring system.
Leukemia, 20(4) 2006, 620-26.
(PMID 16437134)
|
|
| banding: 1 |
Sheth FJ, Sheth JJ, and Desai C.
Case of near triploidy with i(17)(q10) in blast crisis CML.
Cancer Genet Cytogenet, 164(2) 2006, 177-78.
(PMID 16434327)
|
|
| banding: 1 |
Botrus G, Sciot R, and Debiec-Rychter M.
Cutaneous aneurysmal fibrous histiocytoma with a t(12;19)(p12;q13) as the sole cytogenetic anomaly.
Cancer Genet Cytogenet, 164(2) 2006, 155-58.
(PMID 16434321)
|
|
| banding: 2 |
Wong KF, Lam SC, and Leung JN.
Isochromosome 7q in Down syndrome.
Cancer Genet Cytogenet, 164(2) 2006, 152-54.
(PMID 16434320)
|
|
| banding: 6 |
Prat E, Bernues M, Del Rey J, Camps J, Ponsa I, Algaba F, Egozcue J, Caballin MR, et al.
Common pattern of unusual chromosome abnormalities in hereditary papillary renal carcinoma.
Cancer Genet Cytogenet, 164(2) 2006, 142-47.
(PMID 16434318)
|
|
| banding: 1 |
Knutsen T, Vakulchuk A, Mosijczuk AD, Gabrea A, Ried T, and Tretyak N.
Complex rearrangements involving der(8)t(8;20) and der(14)t(8;14)t(11;14), CCND1, and duplication of IgH constant region in acute plasmablastic leukemia.
Cancer Genet Cytogenet, 164(2) 2006, 137-41.
(PMID 16434317)
|
|
| banding: 27 |
Han JY, Theil KS, and Hoeltge G.
Frequencies and characterization of cytogenetically unrelated clones in various hematologic malignancies: seven years of experiences in a single institution.
Cancer Genet Cytogenet, 164(2) 2006, 128-32.
(PMID 16434315)
|
|
| banding: 2 |
Xinh PT, Vu HA, Nghia H, Binh NT, Van Be T, Van Binh T, Tokunaga K, et al.
Coexistence of Philadelphia chromosome positive cells with and without der(9) deletion in a patient with chronic myelogenous leukemia.
Cancer Genet Cytogenet, 164(2) 2006, 122-27.
(PMID 16434314)
|
|
| banding: 1 |
Monma F, Nishii K, Ezuki S, Miyazaki T, Yamamori S, Usui E, Sugimoto Y, Lorenzo VF, et al.
Molecular and phenotypic analysis of Philadelphia chromosome-positive bilineage leukemia: possibility of a lineage switch from T-lymphoid leukemic progenitor to myeloid . . .
Cancer Genet Cytogenet, 164(2) 2006, 118-21.
(PMID 16434313)
|
|
| banding: 1 |
Chen WC, Jones D, Ho CL, Cheng CN, Tseng JY, Tsai HP, and Chang KC.
Cytogenetic anomalies in hyaline vascular Castleman disease: report of two cases with reappraisal of histogenesis.
Cancer Genet Cytogenet, 164(2) 2006, 110-17.
(PMID 16434312)
|
|
| banding: 4 |
Zhang IH, Zane LT, Braun BS, Maize JJ, Zoger S, and Loh ML.
Congenital leukemia cutis with subsequent development of leukemia.
J Am Acad Dermatol, 54(2 Suppl) 2006, S22-7.
(PMID 16427986)
|
|
| banding: 2 |
Soma LA, Gollin SM, Remstein ED, Ketterling RP, Flynn HC, Rajasenan KK, et al.
Splenic small B-cell lymphoma with IGH/BCL3 translocation.
Hum Pathol, 37(2) 2006, 218-30.
(PMID 16426923)
|
|
| banding: 9 |
Hosoya N, Sanada M, Nannya Y, Nakazaki K, Wang L, Hangaishi A, Kurokawa M, Chiba S, et al.
Genomewide screening of DNA copy number changes in chronic myelogenous leukemia with the use of high-resolution array-based comparative genomic hybridization.
Genes Chromosomes Cancer, 45(5) 2006, 482-94.
(PMID 16425296)
|
|
| banding: 1 |
Adelaide J, Perot C, Gelsi-Boyer V, Pautas C, Murati A, Copie-Bergman C, Imbert M, et al.
A t(8;9) translocation with PCM1-JAK2 fusion in a patient with T-cell lymphoma.
Leukemia, 20(3) 2006, 536-37.
(PMID 16424865)
|
|
| banding: 9 |
Matsuda K, Matsuzaki S, Miki J, Hidaka E, Yanagisawa R, Nakazawa Y, Sakashita K, et al.
Chromosomal change during 6-mercaptopurine (6-MP) therapy in juvenile myelomonocytic leukemia: the growth of a 6-MP-refractory clone that already exists at onset.
Leukemia, 20(3) 2006, 485-90.
(PMID 16424864)
|
|
| banding: 2 |
van Zutven LJ, Onen E, Velthuizen SC, van Drunen E, von Bergh AR, et al.
Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene.
Genes Chromosomes Cancer, 45(5) 2006, 437-46.
(PMID 16419055)
|
|
| banding: 1 |
Zhang GS, Dai CW, Peng HL, Xu YX, and Pei MF.
Myelodysplastic syndrome with transformation to acute monocytic leukemia with FLT3-ITD mutation following orthotopic liver transplantation.
Leuk Res, 30(7) 2006, 908-10.
(PMID 16417920)
|
|
| banding: 19 |
Willems SM, Debiec-Rychter M, Szuhai K, Hogendoorn PC, and Sciot R.
Local recurrence of myxofibrosarcoma is associated with increase in tumour grade and cytogenetic aberrations, suggesting a multistep tumour progression model.
Mod Pathol, 19(3) 2006, 407-16.
(PMID 16415793)
|
|
| banding: 8 |
Meyer-Monard S, Parlier V, Passweg J, Muhlematter D, Hess U, Bargetzi M, Kuhne T, et al.
Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia.
Leukemia, 20(2) 2006, 247-53.
(PMID 16408102)
|
|
| banding: 18 |
Haltrich I, Kost-Alimova M, Kovacs G, Klein G, Fekete G, and Imreh S.
Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients.
Eur J Haematol, 76(2) 2006, 124-33.
(PMID 16405433)
|
|
| banding: 3 |
Micci F, Panagopoulos I, Bjerkehagen B, and Heim S.
Consistent rearrangement of chromosomal band 6p21 with generation of fusion genes JAZF1/PHF1 and EPC1/PHF1 in endometrial stromal sarcoma.
Cancer Res, 66(1) 2006, 107-12.
(PMID 16397222)
|
|
| banding: 3 |
Piccaluga PP, Malagola M, Rondoni M, Ottaviani E, Testoni N, Laterza C, Visani G, et al.
Poor outcome of adult acute lymphoblastic leukemia patients carrying the (1;19)(q23;p13) translocation.
Leuk Lymphoma, 47(3) 2006, 469-72.
(PMID 16396770)
|
|
| banding: 2 |
Quilichini B, Andre N, Bouvier C, Chrestian MA, Rome A, Intagliata D, Coze C, Lena G, et al.
Hidden chromosomal abnormalities in pleuropulmonary blastomas identified by multiplex FISH.
BMC Cancer, 6 2006, 4.
(PMID 16396677)
|
|
| banding: 4 |
Huang L, Abruzzo LV, Valbuena JR, Medeiros LJ, and Lin P.
Acute myeloid leukemia associated with variant t(8;21) detected by conventional cytogenetic and molecular studies: a report of four cases and review of the literature.
Am J Clin Pathol, 125(2) 2006, 267-72.
(PMID 16393685)
|
|
| banding: 5 |
Wu Y, Slovak ML, Snyder DS, and Arber DA.
Coexistence of inversion 16 and the Philadelphia chromosome in acute and chronic myeloid leukemias : report of six cases and review of literature.
Am J Clin Pathol, 125(2) 2006, 260-66.
(PMID 16393682)
|
|
| banding: 10 |
Batista DA, Vonderheid EC, Hawkins A, Morsberger L, Long P, Murphy KM, et al.
Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sezary syndrome: search for recurrent chromosome abnormalities.
Genes Chromosomes Cancer, 45(4) 2006, 383-91.
(PMID 16382449)
|
|
| banding: 5 |
Maserati E, Minelli A, Pressato B, Valli R, Crescenzi B, Stefanelli M, Menna G, et al.
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Genes Chromosomes Cancer, 45(4) 2006, 375-82.
(PMID 16382447)
|
|
| banding: 1 |
Yinjun L, Jie J, and Zhimei C.
Granulocytic sarcoma of the gingiva with trisomy 21.
Am J Hematol, 81(1)(1) 2006, 79-80.
(PMID 16369955)
|
|
| banding: 1 |
Potenza L, Luppi M, Riva G, Morselli M, Ferrari A, Imovilli A, Giacobbi F, et al.
Isolated extramedullary relapse after autologous bone marrow transplantation for acute myeloid leukemia: case report and review of the literature.
Am J Hematol, 81(1) 2006, 45-50.
(PMID 16369953)
|
|
| banding: 1 |
Hameed M, Chen F, Mahmet K, Das K, and Kim S.
Schwannoma with a reciprocal t(9;22)(q22;q13).
Cancer Genet Cytogenet, 164(1)(1) 2006, 92-93.
(PMID 16364772)
|
|
| banding: 1 |
Nunoda K, Sashida G, Ohyashiki K, Kodama A, and Fukutake K.
The translocation (4;12)(q31;q21) in myelofibrosis associated with myelodysplastic syndrome: impact of the 12q21 breakpoint.
Cancer Genet Cytogenet, 164(1)(1) 2006, 90-91.
(PMID 16364771)
|
|
| banding: 7 |
Andrieux J, Geffroy S, Bilhou-Nabera C, Dupriez B, Demory JL, Bauters F, Lai JL, et al.
Cryptic 6p21.3 duplications and triplication involving HMGA1 partially masked by add 6p in four cases of myelodysplasia.
Cancer Genet Cytogenet, 164(1) 2006, 84-87.
(PMID 16364769)
|
|
| banding: 1 |
Haltrich I, Kost-Alimova M, Kovacs G, Krivan G, Tamaska J, Klein G, Fekete G, et al.
Jumping translocation of 17q11 approximately qter and 3q25 approximately q28 duplication in a variant Philadelphia t(9;14;22)(q34;q32;q11) in a childhood chronic myelogenous . . .
Cancer Genet Cytogenet, 164(1) 2006, 74-80.
(PMID 16364767)
|
|
| banding: 11 |
Berger R, Busson M, Dastugue N, Radford-Weiss I, Michaux L, Hagemeijer A, et al.
Acute megakaryoblastic leukemia and loss of the RUNX1 gene.
Cancer Genet Cytogenet, 164(1) 2006, 71-73.
(PMID 16364766)
|
|
| banding: 1 |
Kempski HM, Austin N, Chatters SJ, Toomey SM, Chalker J, Anderson J, et al.
Previously unidentified complex cytogenetic changes found in a pediatric case of solid-pseudopapillary neoplasm of the pancreas.
Cancer Genet Cytogenet, 164(1) 2006, 54-60.
(PMID 16364763)
|
|
| banding: 46 |
Jin C, Jin Y, Wennerberg J, Annertz K, Enoksson J, and Mertens F.
Cytogenetic abnormalities in 106 oral squamous cell carcinomas.
Cancer Genet Cytogenet, 164(1) 2006, 44-53.
(PMID 16364762)
|
|
| banding: 2 |
Paulsson K, Bekassy AN, Olofsson T, Mitelman F, Johansson B, et al.
A novel and cytogenetically cryptic t(7;21)(p22;q22) in acute myeloid leukemia results in fusion of RUNX1 with the ubiquitin-specific protease gene USP42.
Leukemia, 20(2) 2006, 224-29.
(PMID 16357831)
|
|
| banding: 35 |
Poppe B, Dastugue N, Vandesompele J, Cauwelier B, De Smet B, Yigit N, De Paepe A, et al.
EVI1 is consistently expressed as principal transcript in common and rare recurrent 3q26 rearrangements.
Genes Chromosomes Cancer, 45(4) 2006, 349-56.
(PMID 16342172)
|
|
| banding: 3 |
Shih LY, Liang DC, Fu JF, Wu JH, Wang PN, Lin TL, Dunn P, Kuo MC, Tang TC, Lin TH, et al.
Characterization of fusion partner genes in 114 patients with de novo acute myeloid leukemia and MLL rearrangement.
Leukemia, 20(2) 2006, 218-23.
(PMID 16341046)
|
|
| banding: 1 |
Streubel B, Vinatzer U, Willheim M, Raderer M, and Chott A.
Novel t(5;9)(q33;q22) fuses ITK to SYK in unspecified peripheral T-cell lymphoma.
Leukemia, 20(2) 2006, 313-18.
(PMID 16341044)
|
|
| banding: 1 |
Redner RL, Contis LC, Craig F, Evans C, Sherer ME, and Shekhter-Levin S.
A novel t(3;17)(p25;q21) variant translocation of acute promyelocytic leukemia with rearrangement of the RARA locus.
Leukemia, 20(2) 2006, 376-79.
(PMID 16341036)
|
|
| banding: 8 |
Ossard-Receveur A, Bernheim A, Clausse B, Danglot G, Fauvet D, Leon B, Lozach F, et al.
Duplication of the Ph-chromosome as a possible mechanism of resistance to imatinib mesylate in patients with chronic myelogenous leukemia.
Cancer Genet Cytogenet, 163(2)(2) 2005, 189-90.
(PMID 16337868)
|
|
| banding: 1 |
Abdelmoula NB, Landman-Parker J, Tourniaire B, Josset P, Boccon-Gibod L, Peter M, et al.
An aggressive Ewing sarcoma associated with a new variant translocation, t(4;11;22)(q25;q24;q12), hyperdiploid karyotype, and tetrasomy 8.
Cancer Genet Cytogenet, 163(2) 2005, 186-88.
(PMID 16337867)
|
|
| banding: 1 |
Ferro Delgado MT, Talavera M, Garcia-Miguel P, Sordo MT, Villalon C, Leon A, et al.
Trisomy 2 as the sole karyotypic abnormality in a lymphoproliferative disorder post-liver transplant.
Cancer Genet Cytogenet, 163(2) 2005, 184-85.
(PMID 16337866)
|
|
| banding: 12 |
Davidsson J, Paulsson K, and Johansson B.
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
Cancer Genet Cytogenet, 163(2) 2005, 180-83.
(PMID 16337865)
|
|
| banding: 2 |
MacKinnon RN and Campbell LJ.
A comparison of two contrasting recurrent isochromosomes 20 found in myelodysplastic syndromes suggests that retention of proximal 20q is a significant factor in myeloid . . .
Cancer Genet Cytogenet, 163(2) 2005, 176-79.
(PMID 16337864)
|
|
| banding: 1 |
Fugazza G, Garuti A, Marchelli S, Miglino M, Bruzzone R, Gatti AM, Castello S, et al.
Masked Philadelphia chromosome due to atypical BCR/ABL localization on the 9q34 band and duplication of the der(9) in a case of chronic myelogenous leukemia.
Cancer Genet Cytogenet, 163(2) 2005, 173-75.
(PMID 16337863)
|
|
| banding: 1 |
Salido M, Lloreta J, Melero C, Garcia M, Placer J, Espinet B, Villa O, Bielsa O, et al.
Insertion (8;11) in a renal oncocytoma with multifocal transformation to chromophobe renal cell carcinoma.
Cancer Genet Cytogenet, 163(2) 2005, 160-63.
(PMID 16337860)
|
|
| banding: 1 |
Dincol G, Palanduz S, Nalcaci M, Ucur A, and Buyukaydin B.
Myeloid/natural killer cell precursor acute leukemia with tetraploidy.
Cancer Genet Cytogenet, 163(2) 2005, 156-59.
(PMID 16337859)
|
|
| banding: 2 |
Cerveira N, Torres L, Ribeiro FR, Henrique R, Pinto A, Bizarro S, Ferreira AM, et al.
Multimodal genetic diagnosis of solid variant alveolar rhabdomyosarcoma.
Cancer Genet Cytogenet, 163(2) 2005, 138-43.
(PMID 16337856)
|
|
| banding: 56 |
Lessard M, Struski S, Leymarie V, Flandrin G, Lafage-Pochitaloff M, Mozziconacci MJ, et al.
Cytogenetic study of 75 erythroleukemias.
Cancer Genet Cytogenet, 163(2) 2005, 113-22.
(PMID 16337853)
|
|
| banding: 33 |
Scholl C, Schlenk RF, Eiwen K, Dohner H, Frohling S, and Dohner K.
The prognostic value of MLL-AF9 detection in patients with t(9;11)(p22;q23)-positive acute myeloid leukemia.
Haematologica, 90(12) 2005, 1626-34.
(PMID 16330435)
|
|
| banding: 2 |
Rakheja D, Kapur P, Tomlinson GE, and Margraf LR.
Pediatric renal cell carcinomas with Xp11.2 rearrangements are immunoreactive for hMLH1 and hMSH2 proteins.
Pediatr Dev Pathol, 8(6) 2005, 615-20.
(PMID 16328670)
|
|
| banding: 4 |
Lefevre M, Couturier J, Sibony M, Bazille C, Boyer K, Callard P, Vieillefond A, et al.
Adult papillary renal tumor with oncocytic cells: clinicopathologic, immunohistochemical, and cytogenetic features of 10 cases.
Am J Surg Pathol, 29(12) 2005, 1576-81.
(PMID 16327429)
|
|
| banding: 1 |
Coupland LA, Brun M, Jammu V, and DRozario JM.
A variant chronic B-cell lymphoma characterized by villous cells with novel immunophenotypic and cytogenetic profiles.
Leuk Lymphoma, 47(1) 2006, 129-34.
(PMID 16321837)
|
|
| banding: 1 |
Finn WG, Sreekumar A, Menon A, Utiger C, and Chinnaiyan A.
Trisomy 12-associated, t(11;14)-negative mature B-cell leukemia with gene expression profile resembling mantle cell lymphoma.
Leuk Lymphoma, 47(1) 2006, 121-27.
(PMID 16321836)
|
|
| banding: 9 |
Christacos NC, Quade BJ, Dal Cin P, and Morton CC.
Uterine leiomyomata with deletions of Ip represent a distinct cytogenetic subgroup associated with unusual histologic features.
Genes Chromosomes Cancer, 45(3) 2006, 304-12.
(PMID 16320247)
|
|
| banding: 2 |
Neas K, Peters G, Jackson J, Tembe M, Wu ZH, Brohede J, Hannan GN, et al.
Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association.
Clin Dysmorphol, 15(1) 2006, 1-8.
(PMID 16317299)
|
|
| banding: 5 |
Brandal P, Bjerkehagen B, and Heim S.
Rearrangement of chromosomal region 8q11-13 in lipomatous tumours: correlation with lipoblastoma morphology.
J Pathol, 208(3) 2006, 388-94.
(PMID 16308870)
|
|
| banding: 1 |
Kajtar B, Deak L, Kalasz V, Pajor L, Molnar L, and Mehes G.
Multiple constitutional chromosome translocations of familial nature in Philadelphia chromosome-positive chronic myeloid leukemia: a report on a unique case.
Int J Hematol, 82(4) 2005, 347-50.
(PMID 16298829)
|
|
| banding: 2 |
Chang YH, Park J, Kim HC, Chun HK, Kim YR, Kim M, Han K, Lee JH, Lee KH, Cho HI, et al.
Korean patients with chronic lymphocytic leukemia show the similar types of chromosomal aberrations as those in Europe and North America.
Leuk Res, 30(6) 2006, 695-99.
(PMID 16297977)
|
|
| banding: 3 |
Storlazzi CT, Wozniak A, Panagopoulos I, Sciot R, Mandahl N, Mertens F, et al.
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22).
Int J Cancer, 118(8) 2006, 1972-76.
(PMID 16284948)
|
|
| banding: 19 |
Djokic M, Le Beau MM, Swinnen LJ, Smith SM, Rubin CM, Anastasi J, et al.
Post-transplant lymphoproliferative disorder subtypes correlate with different recurring chromosomal abnormalities.
Genes Chromosomes Cancer, 45(3) 2006, 313-18.
(PMID 16283619)
|
|
| banding: 1 |
Tyybakinoja A, Saarinen-Pihkala U, Elonen E, and Knuutila S.
Amplified, lost, and fused genes in 11q23-25 amplicon in acute myeloid leukemia, an array-CGH study.
Genes Chromosomes Cancer, 45(3) 2006, 257-64.
(PMID 16283618)
|
|
| banding: 8 |
Nilsson M, Mertens F, Hoglund M, Mandahl N, and Panagopoulos I.
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
Cytogenet Genome Res, 112(1-2) 2006, 60-66.
(PMID 16276091)
|
|
| banding: 1 |
Hato A, Murayama T, Nishikawa S, Kajimoto K, Gomyo H, Sugimoto T, Mizuno I, et al.
Philadelphia chromosome positive acute lymphoblastic leukemia showing normal karyotype in G-banding chromosomal examination before chemotherapy.
Hematology, 10(5) 2005, 379-81.
(PMID 16273725)
|
|
| banding: 1 |
Douet-Guilbert N, Morel F, Le Bris MJ, and De Braekeleer M.
Identification of a complex (11;17;15) translocation in acute promyelocytic leukemia.
Cancer Genet Cytogenet, 163(1) 2005, 93-94.
(PMID 16271965)
|
|
| banding: 1 |
Lau LC, Koh LP, Lim TH, Loo LE, and Tien SL.
A cryptic three-way translocation involving chromosomes 8, 14, and 21 in a case of acute myeloid leukemia subtype M1.
Cancer Genet Cytogenet, 163(1) 2005, 86-90.
(PMID 16271963)
|
|
| banding: 1 |
Al-Saleem T, Balsara BR, Liu Z, Feder M, Testa JR, Wu H, and Greenberg RE.
Renal oncocytoma with loss of chromosomes Y and 1 evolving to papillary carcinoma in connection with gain of chromosome 7. Coincidence or progression?
Cancer Genet Cytogenet, 163(1) 2005, 81-85.
(PMID 16271962)
|
|
| banding: 1 |
Oren H, Yuksel E, Yilmaz S, Turker M, Demircioglu F, and Irken G.
Poor clinical course in a child with myelodysplastic syndrome and del(13)(q14q22).
Cancer Genet Cytogenet, 163(1) 2005, 74-76.
(PMID 16271960)
|
|
| banding: 1 |
Ferguson EC, Talley P, and Vora A.
Translocation (6;17)(q23;q11.2): a novel cytogenetic abnormality in congenital acute myeloid leukemia?
Cancer Genet Cytogenet, 163(1) 2005, 71-73.
(PMID 16271959)
|
|
| banding: 2 |
Kozlov I, Beason K, Yu C, and Hughson M.
CD79a expression in acute myeloid leukemia t(8;21) and the importance of cytogenetics in the diagnosis of leukemias with immunophenotypic ambiguity.
Cancer Genet Cytogenet, 163(1) 2005, 62-67.
(PMID 16271957)
|
|
| banding: 21 |
Yoo SJ, Chi HS, Jang S, Seo EJ, Seo JJ, Lee JH, Park HS, and Park CJ.
Quantification of AML1-ETO fusion transcript as a prognostic indicator in acute myeloid leukemia.
Haematologica, 90(11) 2005, 1493-501.
(PMID 16266896)
|
|
| banding: 1 |
Kanazawa T, Ogawa C, Taketani T, Taki T, Hayashi Y, and Morikawa A.
TLS/FUS-ERG fusion gene in acute lymphoblastic leukemia with t(16;21)(p11;q22) and monitoring of minimal residual disease.
Leuk Lymphoma, 46(12) 2005, 1833-35.
(PMID 16263589)
|
|
| banding: 1 |
Pawarode A, Baer MR, Padmanabhan S, Wallace PK, Barcos M, Sait SN, Block AW, et al.
Simultaneous presentation of acute monoblastic leukemia and mantle cell lymphoma: case report and review of the literature.
Leuk Lymphoma, 46(12) 2005, 1813-18.
(PMID 16263586)
|
|
| banding: 2 |
Daly K, Nandula SV, Murty VV, and Nichols G.
Variant translocation with a deletion of derivative (9q) in a case of Philadelphia chromosome positive (Ph +) essential thrombocythemia (ET), a variant of chronic myelogenous leukemia (CML) . . .
Leuk Lymphoma, 46(12) 2005, 1801-06.
(PMID 16263584)
|
|
| banding: 1 |
Espinet B, Sole F, Pedro C, Garcia M, Bellosillo B, Salido M, Florensa L, Camacho FI, et al.
Clonal proliferation of cyclin D1-positive mantle lymphocytes in an asymptomatic patient: an early-stage event in the development or an indolent form of a mantle cell . . .
Hum Pathol, 36(11) 2005, 1232-37.
(PMID 16260278)
|
|
| banding: 12 |
Kanungo A, Medeiros LJ, Abruzzo LV, and Lin P.
Lymphoid neoplasms associated with concurrent t(14;18) and 8q24/c-MYC translocation generally have a poor prognosis.
Mod Pathol, 19(1) 2006, 25-33.
(PMID 16258503)
|
|
| banding: 23 |
Schnittger S, Kohl TM, Haferlach T, Kern W, Hiddemann W, Spiekermann K, et al.
KIT-D816 mutations in AML1-ETO-positive AML are associated with impaired event-free and overall survival.
Blood, 107(5) 2006, 1791-99.
(PMID 16254134)
|
|
| banding: 1 |
Gorschluter M, Mey U, Glasmacher A, Schwerdtfeger R, and Schmidt-Wolf IG.
Acute myeloid leukemia with near-triploid karyotype and extramedullary involvement of mediastinum.
Bone Marrow Transplant, 36(12) 2005, 1107.
(PMID 16247438)
|
|
| banding: 2 |
Heiss S, Erdel M, Gunsilius E, Nachbaur D, and Tzankov A.
Myelodysplastic/myeloproliferative disease with erythropoietic hyperplasia (erythroid preleukemia) and the unique translocation (8;9)(p23;p24): first description of a . . .
Hum Pathol, 36(10) 2005, 1148-51.
(PMID 16226118)
|
|
| banding: 1 |
Kuchenbauer F, Schoch C, Holler E, Haferlach T, Hiddemann W, et al.
A rare case of acute myeloid leukemia with a CHIC2-ETV6 fusiongen and multiple other molecular aberrations.
Leukemia, 19(12) 2005, 2366-68.
(PMID 16224488)
|
|
| banding: 1 |
Yilmaz Z, Alioglu B, Ozalp O, Yilmaz BT, Ozyurek HE, Ozbek N, et al.
Clonal monosomy 7 in a megakaryoblastic leukemia developed on the basis of Fanconi anemia.
J Pediatr Hematol Oncol, 27(10) 2005, 565-66.
(PMID 16217263)
|
|
| banding: 1 |
Chim CS and Ma SK.
Der(8)t(1;8) in myeloblastic transformation of ET with hydroxyurea as the sole prior treatment.
Hematol Oncol, 23(2) 2005, 57-60.
(PMID 16216034)
|
|
| banding: 1 |
Jarosova M, Takacova S, Holzerova M, Priwitzerova M, Divoka M, Lakoma I, Mihal V, et al.
Cryptic MLL-AF10 fusion caused by insertion of duplicated 5 part of MLL into 10p12 in acute leukemia: a case report.
Cancer Genet Cytogenet, 162(2) 2005, 179-82.
(PMID 16213369)
|
|
| banding: 1 |
Yamamoto K, Ito M, Minagawa K, Urahama N, Sada A, Okamura A, et al.
A der(13)t(7;13)(p13;q14) with monoallelic loss of RB1 and D13S319 in myelodysplastic syndrome.
Cancer Genet Cytogenet, 162(2) 2005, 160-65.
(PMID 16213365)
|
|
| banding: 15 |
Perez-Vera P, Montero-Ruiz O, Frias S, Ulloa-Aviles V, Cardenas-Cardos R, et al.
Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single . . .
Cancer Genet Cytogenet, 162(2) 2005, 140-45.
(PMID 16213362)
|
|
| banding: 7 |
Chen Z, Pasquini M, Hong B, DeHart S, Heikens M, and Tsai S.
The human Penumbra gene is mapped to a region on chromosome 7 frequently deleted in myeloid malignancies.
Cancer Genet Cytogenet, 162(2) 2005, 95-98.
(PMID 16213355)
|
|
| banding: 6 |
Ellison DA, Parham DM, and Sawyer JR.
Cytogenetic findings in pediatric T-lymphoblastic lymphomas: one institutions experience and a review of the literature.
Pediatr Dev Pathol, 8(5) 2005, 550-56.
(PMID 16211447)
|
|
| banding: 10 |
Sanjmyatav J, Schubert J, and Junker K.
Comparative study of renal cell carcinoma by CGH, multicolor-FISH and conventional cytogenic banding analysis.
Oncol Rep, 14(5) 2005, 1183-87.
(PMID 16211283)
|
|
| banding: 1 |
Rudduck-Sivaswaren C, Tien SL, Lim P, Lim E, Lie DK, Tan PH, and Lee AS.
Evidence for deletion of 9q as a two-step process in chronic myeloid leukemia.
Clin Genet, 68(5) 2005, 461-65.
(PMID 16207215)
|
|
| banding: 1 |
Sperr WR, Drach J, Hauswirth AW, Ackermann J, Mitterbauer M, Mitterbauer G, et al.
Myelomastocytic leukemia: evidence for the origin of mast cells from the leukemic clone and eradication by allogeneic stem cell transplantation.
Clin Cancer Res, 11(19 Pt 1) 2005, 6787-92.
(PMID 16203765)
|
|
| banding: 5 |
Merzianu M, Medeiros LJ, Cortes J, Yin C, Lin P, Jones D, Glassman A, Kantarjian H, et al.
inv(16)(p13q22) in chronic myelogenous leukemia in blast phase: a clinicopathologic, cytogenetic, and molecular study of five cases.
Am J Clin Pathol, 124(5) 2005, 807-14.
(PMID 16203287)
|
|
| banding: 3 |
Jabbour E, Kantarjian H, OBrien S, Rios MB, Abruzzo L, Verstovsek S, Garcia-Manero G, et al.
Sudden blastic transformation in patients with chronic myeloid leukemia treated with imatinib mesylate.
Blood, 107(2) 2006, 480-82.
(PMID 16195326)
|
|
| banding: 1 |
Rack K, Delannoy A, Ravoet C, Vannuffel P, Hamels J, and Gillerot Y.
Translocation of BCL2 and BCL6 to the same immunoglobulin heavy chain locus in a case of follicular lymphoma.
Leuk Lymphoma, 46(10) 2005, 1513-16.
(PMID 16194898)
|
|
| banding: 1 |
Kelley TW, Prayson RA, Barnett GH, Stevens GH, Cook JR, and Hsi ED.
Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue arising in the lateral ventricle.
Leuk Lymphoma, 46(10) 2005, 1423-27.
(PMID 16194887)
|
|
| banding: 2 |
Crowley JA, Wang Y, Rapoport AP, and Ning Y.
Detection of MOZ-CBP fusion in acute myeloid leukemia with 8;16 translocation.
Leukemia, 19(12) 2005, 2344-45.
(PMID 16193081)
|
|
| banding: 26 |
Einerson RR, Kurtin PJ, Dayharsh GA, Kimlinger TK, and Remstein ED.
FISH is superior to PCR in detecting t(14;18)(q32;q21)-IgH/bcl-2 in follicular lymphoma using paraffin-embedded tissue samples.
Am J Clin Pathol, 124(3) 2005, 421-29.
(PMID 16191511)
|
|
| banding: 33 |
Mayr C, Speicher MR, Kofler DM, Buhmann R, Strehl J, Busch R, Hallek M, et al.
Chromosomal translocations are associated with poor prognosis in chronic lymphocytic leukemia.
Blood, 107(2) 2006, 742-51.
(PMID 16179374)
|
|
| banding: 1 |
Toubai T, Tanaka J, Higa T, Iwao N, Shigematsu A, Kato N, Watanabe K, Sudo J, et al.
t(1:3)(q10;p10) and chromosome 7 abnormality associated with the progression of multiple myeloma.
Clin Lab Haematol, 27(5) 2005, 355-56.
(PMID 16178923)
|
|
| banding: 1 |
Durrant E, Diaz S, Greenaway S, and Smith A.
A novel cytogenetic abnormality in Burkitt lymphoma associated with treatment resistant disease.
Clin Lab Haematol, 27(5) 2005, 328-30.
(PMID 16178915)
|
|
| banding: 1 |
Hamadani M, Tfayli A, Sethi S, Awab A, and Hamdani N.
Granulocytic sarcoma manifesting as multiple skeletal lesions.
Am J Med Sci, 330(3) 2005, 139-43.
(PMID 16174998)
|
|
| banding: 1 |
Yamamoto K, Nishikawa S, Minagawa K, Yakushijin K, Okamura A, et al.
Therapy-related myelodysplastic syndrome with inv(16)(p13q22) and I type CBFbeta/MYH11 after autologous transplantation: undetectable fusion transcript in pretransplant progenitor . . .
Leuk Res, 30(3) 2006, 354-61.
(PMID 16165210)
|
|
| banding: 16 |
Hsiao HH, Ito Y, Sashida G, Ohyashiki JH, and Ohyashiki K.
De novo appearance of der(1;7)(q10;p10) is associated with leukemic transformation and unfavorable prognosis in essential thrombocythemia.
Leuk Res, 29(11) 2005, 1247-52.
(PMID 16164981)
|
|
| banding: 1 |
Sai P, Kalavar M, Raval M, Sipot CR, and Steier W.
A case of chronic neutrophilic leukemia with novel chromosomal abnormalities.
Clin Adv Hematol Oncol, 2(8) 2004, 543-; discussion 545.
(PMID 16163234)
|
|
| banding: 1 |
Panagopoulos I, Nilsson T, Domanski HA, Isaksson M, Lindblom P, Mertens F, et al.
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
Int J Cancer, 118(5) 2006, 1181-86.
(PMID 16161041)
|
|
| banding: 1 |
Nakano S, Namura K, Uchida R, Fuchida S, Okano A, Okamoto M, et al.
The unbalanced chromosomal translocation der(15)t(1;15)(q21;p13) in multiple myeloma.
Int J Hematol, 81(5) 2005, 437-38.
(PMID 16158828)
|
|
| banding: 1 |
Kitazawa J, Tono C, Terui K, Kinukawa N, Oda M, Isoyama K, Ishii E, et al.
Successful outcome of mismatched hematopoietic stem cell transplantation from a related donor in an infant with acute lymphoblastic leukemia and 9;11 translocation: case report and review of . . .
Int J Hematol, 81(5) 2005, 428-32.
(PMID 16158826)
|
|
| banding: 1 |
Kozon LK, Wesley DL, Van Brunt Jr, and Li MM.
A novel interstitial deletion on the long arm of chromosome 16 in a patient with chronic myelomonocytic leukemia.
Cancer Genet Cytogenet, 162(1) 2005, 92-94.
(PMID 16157209)
|
|
| banding: 2 |
Ligon AH, DeAngelo DJ, Atkins L, and Dal Cin P.
Isochromosome of a deleted 20q may be a relatively common abnormality in myeloid malignancies.
Cancer Genet Cytogenet, 162(1) 2005, 89-91.
(PMID 16157208)
|
|
| banding: 2 |
Cook JR, Aguilera NI, Reshmi S, Huang X, Yu Z, Gollin SM, Abbondanzo SL, et al.
Deletion 6q is not a characteristic marker of nodal lymphoplasmacytic lymphoma.
Cancer Genet Cytogenet, 162(1) 2005, 85-88.
(PMID 16157207)
|
|
| banding: 1 |
Poppe B, Yigit N, De Moerloose B, De Paepe A, Benoit Y, and Speleman F.
HOXA gene cluster rearrangement in a t(7;9)(p15;q34) in a child with MDS.
Cancer Genet Cytogenet, 162(1) 2005, 82-84.
(PMID 16157206)
|
|
| banding: 3 |
Nishio J, Reith JD, Ogose A, Maale G, Neff JR, and Bridge JA.
Cytogenetic findings in clear cell chondrosarcoma.
Cancer Genet Cytogenet, 162(1) 2005, 74-77.
(PMID 16157204)
|
|
| banding: 4 |
Sambani C, La Starza R, Pierini V, Vandenberghe P, Gonzales-Aguilera JJ, Rigana H, et al.
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).
Cancer Genet Cytogenet, 162(1) 2005, 45-49.
(PMID 16157199)
|
|
| banding: 3 |
Dave BJ, Wiggins M, Higgins CM, Pickering DL, Perry D, Aoun P, Abromowich M, et al.
9q34 rearrangements in BCR/ABL fusion-negative acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 162(1) 2005, 30-37.
(PMID 16157197)
|
|
| banding: 41 |
Alvarez Y, Coll MD, Ortega JJ, Bastida P, Dastugue N, Robert A, Cervera J, et al.
Genetic abnormalities associated with the t(12;21) and their impact in the outcome of 56 patients with B-precursor acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 162(1) 2005, 21-29.
(PMID 16157196)
|
|
| banding: 17 |
Aamot HV, Micci F, Holte H, Delabie J, and Heim S.
G-banding and molecular cytogenetic analyses of marginal zone lymphoma.
Br J Haematol, 130(6) 2005, 890-901.
(PMID 16156859)
|
|
| banding: 5 |
Aamot HV, Bjornslett M, Delabie J, and Heim S.
t(14;22)(q32;q11) in non-Hodgkin lymphoma and myeloid leukaemia: molecular cytogenetic investigations.
Br J Haematol, 130(6) 2005, 845-51.
(PMID 16156854)
|
|
| banding: 7 |
Poppe B, Cauwelier B, Van Limbergen H, Yigit N, Philippe J, Verhasselt B, De Paepe A, et al.
Novel cryptic chromosomal rearrangements in childhood acute lymphoblastic leukemia detected by multiple color fluorescent in situ hybridization.
Haematologica, 90(9) 2005, 1179-85.
(PMID 16154840)
|
|
| banding: 6 |
Vranova V, Katina S, Kirschnerova G, Mistrik M, Lakota J, Horakova J, et al.
A significance of additional chromosomal aberrations and other variables on post transplantation outcome of patients with CML.
Neoplasma, 52(5) 2005, 381-87.
(PMID 16151581)
|
|
| banding: 1 |
Corm S, Biggio V, Roche-Lestienne C, Lai JL, Yakoub-Agha I, Philippe N, Nicolini FE, et al.
Coexistence of AML1/RUNX1 and BCR-ABL point mutations in an imatinib-resistant form of CML.
Leukemia, 19(11) 2005, 1991-92.
(PMID 16151468)
|
|
| CGH: 9
banding: 11 |
Langdon JA, Lamont JM, Scott DK, Dyer S, Prebble E, Bown N, Grundy RG, Ellison DW, et al.
Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma.
Genes Chromosomes Cancer, 45(1) 2006, 47-60.
(PMID 16149064)
|
|
| banding: 1 |
Yamamoto S, Nishi M, Taniguchi K, Imayoshi M, Ogata Y, Iwanaga M, Sakai N, et al.
Partial tandem duplication of MLL gene in acute myeloid leukemia with translocation (11;17)(q23;q12-21).
Am J Hematol, 80(1) 2005, 46-49.
(PMID 16138343)
|
|
| banding: 3 |
Molina A, Zain J, Arber DA, Angelopolou M, ODonnell M, Murata-Collins J, Forman SJ, et al.
Durable clinical, cytogenetic, and molecular remissions after allogeneic hematopoietic cell transplantation for refractory Sezary syndrome and mycosis fungoides.
J Clin Oncol, 23(25) 2005, 6163-71.
(PMID 16135483)
|
|
| banding: 2 |
Nilsson M, Panagopoulos I, Mertens F, and Mandahl N.
Fusion of the HMGA2 and NFIB genes in lipoma.
Virchows Arch, 447(5) 2005, 855-58.
(PMID 16133369)
|
|
| banding: 1 |
Surace C, Storlazzi CT, Engellau J, Domanski HA, Gustafson P, Panagopoulos I, et al.
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
Virchows Arch, 447(5) 2005, 869-74.
(PMID 16133367)
|
|
| banding: 1 |
Moid F, Day E, Schneider MA, Goldstein K, and DePalma L.
An indolent case of T-prolymphocytic leukemia with t(3;22)(q21;q11.2) and elevated serum beta2-microglobulin.
Arch Pathol Lab Med, 129(9) 2005, 1164-67.
(PMID 16119992)
|
|
| banding: 17 |
Chen W, Jones D, Medeiros LJ, Luthra R, and Lin P.
Acute myeloid leukaemia with FLT3 gene mutations of both internal tandem duplication and point mutation type.
Br J Haematol, 130(5) 2005, 726-28.
(PMID 16115128)
|
|
| banding: 1 |
Morerio C, Rapella A, Tassano E, Rosanda C, and Panarello C.
MLL-MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia.
Leuk Res, 29(10) 2005, 1223-26.
(PMID 16111539)
|
|
| banding: 1 |
Suzukawa K, Shimizu S, Nemoto N, Takei N, Taki T, and Nagasawa T.
Identification of a chromosomal breakpoint and detection of a novel form of an MLL-AF17 fusion transcript in acute monocytic leukemia with t(11;17)(q23;q21).
Int J Hematol, 82(1) 2005, 38-41.
(PMID 16105757)
|
|
| banding: 1 |
Kim M, Lim J, Lee A, Park G, Kim Y, Han K, Kang CS, Kim YJ, and Song JS.
A case of chronic myelomonocytic leukemia with severe eosinophilia having t(5;12)(q31;p13) with t(1;7)(q10;p10).
Acta Haematol, 114(2) 2005, 104-07.
(PMID 16103634)
|
|
| banding: 19 |
Iliszko M, Kuzniacka A, Lachinski A, Babinska M, Kobierska-Gulida G, et al.
Karyotypic characterization of 64 nonmalignant thyroid goiters.
Cancer Genet Cytogenet, 161(2) 2005, 178-80.
(PMID 16102591)
|
|
| banding: 1 |
Espinoza JP, Cardenas VJ, Luna CA, Fuentes HM, Camacho GV, Carrera FM, et al.
Loss of 10p material in a child with human papillomavirus-positive disseminated bilateral retinoblastoma.
Cancer Genet Cytogenet, 161(2) 2005, 146-50.
(PMID 16102585)
|
|
| banding: 4 |
MacKinnon RN, Zordan A, and Campbell LJ.
Recurrent duplication of Xq27-qter in hematological malignancies revealed by multicolor fluorescence in situ hybridization and multicolor banding.
Cancer Genet Cytogenet, 161(2) 2005, 125-29.
(PMID 16102582)
|
|
| banding: 8 |
Cremer FW, Kartal M, Hose D, Bila J, Buck I, Bellos F, Raab MS, Brough M, Moebus A, et al.
High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH.
Cancer Genet Cytogenet, 161(2) 2005, 116-24.
(PMID 16102581)
|
|
| banding: 26 |
Arnaud B, Douet-Guilbert N, Morel F, Le Bris MJ, Herry A, Banzakour S, Bourquard P, et al.
Screening by fluorescence in situ hybridization for MLL status at diagnosis in 239 unselected patients with acute myeloblastic leukemia.
Cancer Genet Cytogenet, 161(2) 2005, 110-15.
(PMID 16102580)
|
|
| banding: 4 |
Brock JE, Perez-Atayde AR, Kozakewich HP, Richkind KE, Fletcher JA, et al.
Cytogenetic aberrations in perineurioma: variation with subtype.
Am J Surg Pathol, 29(9) 2005, 1164-69.
(PMID 16096405)
|
|
| banding: 9 |
Callet-Bauchu E, Baseggio L, Felman P, Traverse-Glehen A, Berger F, Morel D, Gazzo S, et al.
Cytogenetic analysis delineates a spectrum of chromosomal changes that can distinguish non-MALT marginal zone B-cell lymphomas among mature B-cell entities: a description of 103 . . .
Leukemia, 19(10) 2005, 1818-23.
(PMID 16094418)
|
|
| banding: 2 |
Bousquet M, Quelen C, De Mas V, Duchayne E, Roquefeuil B, Delsol G, Laurent G, et al.
The t(8;9)(p22;p24) translocation in atypical chronic myeloid leukaemia yields a new PCM1-JAK2 fusion gene.
Oncogene, 24(48) 2005, 7248-52.
(PMID 16091753)
|
|
| banding: 3 |
Cross NA, Rennie IG, Murray AK, and Sisley K.
The identification of chromosome abnormalities associated with the invasive phenotype of uveal melanoma in vitro.
Clin Exp Metastasis, 22(2) 2005, 107-13.
(PMID 16086231)
|
|
| banding: 1 |
Song SY, Ko YH, and Ahn G.
Mediastinal germ cell tumor associated with histiocytic sarcoma of spleen: case report of an unusual association.
Int J Surg Pathol, 13(3) 2005, 299-303.
(PMID 16086090)
|
|
| banding: 1 |
Jiang JG, Roman E, Nandula SV, Murty VV, Bhagat G, and Alobeid B.
Congenital MLL-positive B-cell acute lymphoblastic leukemia (B-ALL) switched lineage at relapse to acute myelocytic leukemia (AML) with persistent t(4;11) and t(1;6) translocations and JH . . .
Leuk Lymphoma, 46(8) 2005, 1223-27.
(PMID 16085566)
|
|
| banding: 1 |
Christacos NC, Sherman L, Roy A, DeAngelo DJ, and Dal Cin P.
Is the cryptic interstitial deletion of 8q24 surrounding MYC a common mechanism in the formation of double minute chromosome?
Cancer Genet Cytogenet, 161(1) 2005, 90-92.
(PMID 16080965)
|
|
| banding: 1 |
Meloni-Ehrig AM, Tirado CA, Chen K, Jahn J, Suchan S, Scheerle J, Crosby MG, Meany H, et al.
Isolated del(14)(q21) in a case of precursor B-cell acute lymphoblastic leukemia.
Cancer Genet Cytogenet, 161(1) 2005, 82-85.
(PMID 16080963)
|
|
| banding: 1 |
Tsirigotis P, Papageorgiou S, Abatzis D, Athanatou S, Girkas C, Pappa V, Pangalos C, et al.
Acute myelogenous leukemia with tetrasomy 8 is a disease with a poor prognosis.
Cancer Genet Cytogenet, 161(1) 2005, 78-81.
(PMID 16080962)
|
|
| banding: 1 |
Tirado CA, Jahn JA, Scheerle J, Eid M, Meister RJ, Christie RJ, Croft CD, et al.
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA . . .
Cancer Genet Cytogenet, 161(1) 2005, 70-73.
(PMID 16080960)
|
|
| banding: 6 |
Deeb G, Baer MR, Gaile DP, Sait SN, Barcos M, Wetzler M, Conroy JM, Nowak NJ, et al.
Genomic profiling of myeloid sarcoma by array comparative genomic hybridization.
Genes Chromosomes Cancer, 44(4) 2005, 373-83.
(PMID 16080198)
|
|
| banding: 1 |
Macedo Silva ML, Land M, Heller A, Abdelhay E, do Socorro Pombo-de-Oliveira M, et al.
New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome.
Oncol Rep, 14(3) 2005, 663-66.
(PMID 16077971)
|
|
| banding: 4 |
Patel BB, Mohamed AN, and Schiffer CA.
Acute myelogenous leukemia like translocations in CML blast crisis: two new cases of inv(16)/t(16;16) and a review of the literature.
Leuk Res, 30(2) 2006, 225-32.
(PMID 16076492)
|
|
| banding: 1 |
Nakamura F, Nakamura Y, Maki K, Sato Y, and Mitani K.
Cloning and characterization of the novel chimeric gene TEL/PTPRR in acute myelogenous leukemia with inv(12)(p13q13).
Cancer Res, 65(15) 2005, 6612-21.
(PMID 16061641)
|
|
| banding: 1 |
Hayette S, Cornillet-Lefebvre P, Tigaud I, Struski S, Forissier S, Berchet A, Doll D, et al.
AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partner.
Cancer Res, 65(15) 2005, 6521-25.
(PMID 16061630)
|
|
| banding: 1 |
Daibata M, Taguchi T, Nemoto Y, Iwasaki S, Ohtsuki Y, and Taguchi H.
In vitro Epstein-Barr virus-immortalized lymphoma cell line carrying t(9;14)(p13;q32) chromosome abnormality, derived from splenic lymphoma with villous lymphocytes.
Int J Cancer, 118(2) 2006, 513-17.
(PMID 16049984)
|
|
| banding: 1 |
Srivastava A, Nielsen PG, Dal Cin P, and Rosenberg AE.
Monophasic synovial sarcoma of the liver.
Arch Pathol Lab Med, 129(8) 2005, 1047-49.
(PMID 16048399)
|
|
| banding: 1 |
Disperati P, Ichim CV, Tkachuk D, Chun K, Schuh AC, and Wells RA.
Progression of myelodysplasia to acute lymphoblastic leukaemia: implications for disease biology.
Leuk Res, 30(2) 2006, 233-39.
(PMID 16046234)
|
|
| banding: 1 |
Lam CC, Ma ES, and Kwong YL.
Therapy-related acute myeloid leukemia after single-agent treatment with fludarabine for chronic lymphocytic leukemia.
Am J Hematol, 79(4) 2005, 288-90.
(PMID 16044456)
|
|
| banding: 1 |
Classen CF, Teigler-Schlegel A, Rottgers S, Reinhardt D, Dohner K, et al.
AML bearing the translocation t(11;17)(q23;q21): involvement of MLL and a region close to RARA, with no differentiation response to retinoic acid.
Ann Hematol, 84(12) 2005, 774-80.
(PMID 16044313)
|
|
| banding: 1 |
Ly-Sunnaram B, Henry C, Gandemer V, Mee FL, Burtin F, Blayau M, Cayuela JM, Oster M, et al.
Late ovarian relapse of TEL/AML1 positive ALL confirming that TEL deletion is a secondary event in leukemogenesis.
Leuk Res, 29(9) 2005, 1089-94.
(PMID 16038737)
|
|
| banding: 2 |
Masuko M, Furukawa T, Yersser O, Narita M, Toba K, Koike T, and Aizawa Y.
Persistence of various chromosomal aberrations in recipient cells during complete remission after bone marrow transplantation followed by graft rejection.
Leuk Res, 29(9) 2005, 1083-87.
(PMID 16038736)
|
|
| banding: 1 |
Matsuzaki S, Matsuda K, Miki J, Nakazawa Y, Sakashita K, Kamijo T, Hidaka E, et al.
Development of two cytogenetically abnormal clones from multipotential hematopoietic stem cells in a patient with juvenile myelomonocytic leukemia.
Leuk Res, 29(9) 2005, 1069-72.
(PMID 16038733)
|
|
| banding: 4 |
Murati A, Gelsi-Boyer V, Adelaide J, Perot C, Talmant P, Giraudier S, Lode L, et al.
PCM1-JAK2 fusion in myeloproliferative disorders and acute erythroid leukemia with t(8;9) translocation.
Leukemia, 19(9) 2005, 1692-96.
(PMID 16034466)
|
|
| banding: 7 |
Tosi S, Ballabio E, Teigler-Schlegel A, Boultwood J, Bruch J, et al.
Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute . . .
Genes Chromosomes Cancer, 44(3) 2005, 225-32.
(PMID 16028218)
|
|
| banding: 1 |
Hsiao HH, Sashida G, Ito Y, Tachino M, Beppu H, and Ohyashiki K.
Simultaneous occurrence of der(1;7)(q10;p10) and t(14;18)(q32;q21) in non-Hodgkins lymphoma: der(1;7) will appear as a secondary change in lymphoid neoplasia.
Leuk Lymphoma, 46(6) 2005, 949-50.
(PMID 16019545)
|
|
| banding: 2 |
Millot F, Brizard F, Sorel N, Preudhomme C, Cividin M, Guilhot F, et al.
Therapy-related acute lymphoblastic leukemia with MLL rearrangement following treatment of Burkitts leukemia.
Leuk Lymphoma, 46(6) 2005, 925-27.
(PMID 16019540)
|
|
| banding: 1 |
Scolnik MP, Aranguren PN, Cuello MT, Palacios MF, Sanjurjo J, Giunta M, Bracco MM, et al.
Biphenotypic acute leukemia with t(15;17).
Leuk Lymphoma, 46(4) 2005, 607-10.
(PMID 16019491)
|
|
| banding: 8 |
Sweetser DA, Peniket AJ, Haaland C, Blomberg AA, Zhang Y, Zaidi ST, Dayyani F, et al.
Delineation of the minimal commonly deleted segment and identification of candidate tumor-suppressor genes in del(9q) acute myeloid leukemia.
Genes Chromosomes Cancer, 44(3) 2005, 279-91.
(PMID 16015647)
|
|
| banding: 1 |
Sakai I, Tamura T, Narumi H, Uchida N, Yakushijin Y, Hato T, Fujita S, et al.
Novel RUNX1-PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22).
Genes Chromosomes Cancer S, 44(3) 2005, 265-70.
(PMID 16015645)
|
|
| banding: 1 |
Stergianou K, Fox C, and Russell NH.
Fusion of NUP214 to ABL1 on amplified episomes in T-ALL--implications for treatment.
Leukemia S, 19(9)(9) 2005, 1680-81.
(PMID 16015385)
|
|
| CGH: 1
banding: 1 |
Nishio J, Iwasaki H, Nabeshima K, Ishiguro M, Naumann S, Isayama T, Naito M, et al.
Establishment of a new human epithelioid sarcoma cell line, FU-EPS-1: molecular cytogenetic characterization by use of spectral karyotyping and comparative genomic . . .
Int J Oncol, 27(2) 2005, 361-69.
(PMID 16010416)
|
|
| CGH: 22
banding: 36 |
Karst C, Heller A, Claussen U, Gebhart E, and Liehr T.
Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia.
Int J Oncol, 27(2) 2005, 355-59.
(PMID 16010415)
|
|
| banding: 2 |
Griesinger F, Hennig H, Hillmer F, Podleschny M, Steffens R, Pies A, Wormann B, et al.
A BCR-JAK2 fusion gene as the result of a t(9;22)(p24;q11.2) translocation in a patient with a clinically typical chronic myeloid leukemia.
Genes Chromosomes Cancer, 44(3) 2005, 329-33.
(PMID 16001431)
|
|
| banding: 3 |
Matsuoka H, Murayama T, Koizumi T, Nishimura R, Kawaguchi R, et al.
Establishment of a human myeloid cell line with trisomy 8 derived from overt leukemia following myelodysplastic syndrome.
Haematologica, 90(7)(7) 2005, 981-82.
(PMID 15996938)
|
|
| banding: 6 |
Hertenstein B, Hambach L, Bacigalupo A, Schmitz N, McCann S, Slavin S, Gratwohl A, et al.
Development of leukemia in donor cells after allogeneic stem cell transplantation--a survey of the European Group for Blood and Marrow Transplantation (EBMT).
Haematologica, 90(7) 2005, 969-75.
(PMID 15996934)
|
|
| banding: 1 |
Nakase K, Yamamoto Y, Morita K, Yamaguchi T, Nishii K, and Shiku H.
Haunting appearance of bcr/abl fusion gene products in a patient with therapy related leukaemia.
Leuk Res, 30(1) 2006, 106-08.
(PMID 15996731)
|
|
| banding: 30 |
Brezinova J, Zemanova Z, Ransdorfova S, Sindelarova L, Siskova M, Neuwirtova R, et al.
Prognostic significance of del(20q) in patients with hematological malignancies.
Cancer Genet Cytogenet, 160(2) 2005, 188-92.
(PMID 15993278)
|
|
| banding: 4 |
Bacher U, Haferlach T, and Schoch C.
Gain of 9p due to an unbalanced rearrangement der(9;18): a recurrent clonal abnormality in chronic myeloproliferative disorders.
Cancer Genet Cytogenet, 160(2) 2005, 179-83.
(PMID 15993276)
|
|
| banding: 1 |
Nishio J, Iwasaki H, Althof PA, Naumann S, Ishiguro M, Haraoka S, Iwashita A, et al.
Identification of a ring chromosome with spectral karyotyping in a pleural synovial sarcoma.
Cancer Genet Cytogenet, 160(2) 2005, 174-78.
(PMID 15993275)
|
|
| banding: 5 |
Fuzesi L, Frank D, Nguyen C, Ringert RH, Bartels H, and Gunawan B.
Losses of 1p and chromosome 14 in renal oncocytomas.
Cancer Genet Cytogenet, 160(2) 2005, 120-25.
(PMID 15993267)
|
|
| banding: 10 |
Beyer V, Muhlematter D, Parlier V, Cabrol C, Bougeon-Mamin S, Solenthaler M, et al.
Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of . . .
Cancer Genet Cytogenet, 160(2) 2005, 97-119.
(PMID 15993266)
|
|
| banding: 6 |
Gutierrez-Angulo M, Gonzalez-Garcia JR, Meza-Espinoza JP, Picos-Cardenas VJ, et al.
Increased expression of AML1-a and acquired chromosomal abnormalities in childhood acute lymphoblastic leukemia.
Hematol Oncol, 22(3) 2004, 85-90.
(PMID 15991223)
|
|
| banding: 1 |
Jardin F, Callonnec F, Contentin N, Picquenot JM, Gueit I, Heron F, Bastard C, et al.
Intravascular large B-Cell lymphoma with bone marrow involvement and superior sagittal sinus thrombosis: report of a case successfully treated with a CHOP/rituximab combination . . .
Clin Lymphoma, 6(1) 2005, 46-49.
(PMID 15989707)
|
|
| banding: 1 |
Storlazzi CT, Von Steyern FV, Domanski HA, Mandahl N, and Mertens F.
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma.
Int J Cancer, 117(6) 2005, 1055-57.
(PMID 15986446)
|
|
| banding: 1 |
Grand FH, Koduru P, Cross NC, and Allen SL.
NUP98-LEDGF fusion and t(9;11) in transformed chronic myeloid leukemia.
Leuk Res, 29(12) 2005, 1469-72.
(PMID 15982735)
|
|
| banding: 50 |
Tomlinson GE, Douglass EC, Pollock BH, Finegold MJ, and Schneider NR.
Cytogenetic evaluation of a large series of hepatoblastomas: numerical abnormalities with recurring aberrations involving 1q12-q21.
Genes Chromosomes Cancer, 44(2) 2005, 177-84.
(PMID 15981236)
|
|
| CGH: 2
banding: 2 |
Brandal P, Busund LT, and Heim S.
Chromosome abnormalities in juxtaglomerular cell tumors.
Cancer, 104(3) 2005, 504-10.
(PMID 15968688)
|
|
| banding: 1 |
Scrideli CA, Baruffi MR, Squire JA, Ramos ES, Karaskova J, Heck B, et al.
Acute monocytic leukemia and multiple abnormalities in a child with duplication of 1q detected by GTG-banding and SKY.
Leuk Res, 29(12) 2005, 1465-67.
(PMID 15964069)
|
|
| banding: 10 |
Chang HH, Lu MY, Jou ST, Lin KH, Tien HF, Wu ET, and Lin DT.
Neoplastic disorders of hematopoiesis in children with Downs syndrome--a single institution experience in Taiwan.
J Formos Med Assoc, 104(5) 2005, 333-40.
(PMID 15959600)
|
|
| banding: 2 |
Chen S, Xue Y, Zhang X, Wu Y, Pan J, Wang Y, and Ceng J.
A new human acute monocytic leukemia cell line SHI-1 with t(6;11)(q27;q23), p53 gene alterations and high tumorigenicity in nude mice.
Haematologica, 90(6) 2005, 766-75.
(PMID 15951289)
|
|
| banding: 15 |
Nebral K, Konig M, Schmidt HH, Lutz D, Sperr WR, Kalwak K, Brugger S, Dworzak MN, et al.
Screening for NUP98 rearrangements in hematopoietic malignancies by fluorescence in situ hybridization.
Haematologica, 90(6) 2005, 746-52.
(PMID 15951287)
|
|
| banding: 1 |
Ishii Y, Sashida G, Takaku TI, Sumi M, Nakajima A, and Ohyashiki K.
Cryptic chromosomal anomaly in a patient with acute myeloid leukemia leading to AML1/ETO fusion with unfavorable prognostic factors.
Cancer Genet Cytogenet, 160(1) 2005, 94-95.
(PMID 15949579)
|
|
|
