298 related articles for article (PubMed ID: 16469377)
1. Translocation (13;17)(q14;q25) as a novel chromosomal abnormality in acute myeloid leukemia-M4.
Turhan N; Yürür-Kutlay N; Topcuoglu P; Sayki M; Yüksel M; Gürman G; Tükün A
Leuk Res; 2006 Jul; 30(7):903-5. PubMed ID: 16469377
[TBL] [Abstract][Full Text] [Related]
2. Translocation (11;13)(q23;q14) as the sole abnormality in a childhood de novo acute myelocytic leukemia.
Tsang KS; Li CK; Lau TT; Wong AP; Leung Y; Ng MH
Cancer Genet Cytogenet; 2004 Apr; 150(1):78-80. PubMed ID: 15041229
[TBL] [Abstract][Full Text] [Related]
3. Detection of inv(16) and t(16;16) by fluorescence in situ hybridization in acute myeloid leukemia M4Eo.
Hernández JM; González MB; Granada I; Gutiérrez N; Chillón C; Ramos F; Ribera JM; González M; Feliu E; San Miguel J
Haematologica; 2000 May; 85(5):481-5. PubMed ID: 10800163
[TBL] [Abstract][Full Text] [Related]
4. 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 M4-Eo.
Macedo Silva ML; Raimondi SC; Abdelhay E; Gross M; Mkrtchyan H; de Figueiredo AF; Ribeiro RC; de Jesus Marques-Salles T; Sobral ES; Gerardin Land MP; Liehr T
Cancer Genet Cytogenet; 2008 Apr; 182(1):56-60. PubMed ID: 18328953
[TBL] [Abstract][Full Text] [Related]
5. Acute Myelogeneous Leukemia (M0/M1) with novel chromosomal abnormality of t(14;17) (q32; q11.2).
Ahmad F; Dalvi R; Mandava S; Das BR
Am J Hematol; 2007 Jul; 82(7):676-8. PubMed ID: 17177193
[TBL] [Abstract][Full Text] [Related]
6. Cytogenetics and fluorescence in-situ hybridization in detection of hematological malignancies.
Frenny VJ; Antonella Z; Luisa A; Shah AD; Sheth JJ; Rocchi M
Indian J Cancer; 2003; 40(4):135-9. PubMed ID: 14716109
[TBL] [Abstract][Full Text] [Related]
7. Activation of HLXB9 by juxtaposition with MYB via formation of t(6;7)(q23;q36) in an AML-M4 cell line (GDM-1).
Nagel S; Kaufmann M; Scherr M; Drexler HG; MacLeod RA
Genes Chromosomes Cancer; 2005 Feb; 42(2):170-8. PubMed ID: 15540222
[TBL] [Abstract][Full Text] [Related]
8. Unusual Karyotype in Acute Myelomonocitic Leukemia: A Case Report.
Consoli ML; Romano A; Parrinello NL; Tambè L; Romeo MA; Salemi D; Santoro A; DI Raimondo F
Anticancer Res; 2019 Aug; 39(8):4329-4332. PubMed ID: 31366525
[TBL] [Abstract][Full Text] [Related]
9. Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome.
Manola KN; Panitsas F; Polychronopoulou S; Daraki A; Karakosta M; Stavropoulou C; Avgerinou G; Hatzipantelis E; Pantelias G; Sambani C; Pagoni M
Cancer Genet; 2013 Mar; 206(3):63-72. PubMed ID: 23411131
[TBL] [Abstract][Full Text] [Related]
10. A novel translocation t(1;7)(p36;q34) in three patients with acute myeloid leukaemia.
Specchia G; Cuneo A; Liso V; Contino R; Pastore D; Gentile E; Rocchi M; Castoldi GL
Br J Haematol; 1999 Apr; 105(1):208-14. PubMed ID: 10233385
[TBL] [Abstract][Full Text] [Related]
11. Chromosomal insertion involving MLL in childhood acute myeloblastic leukemia (M4).
Lafay-Cousin L; Soenen V; Mazingue F; Preudhomme C; Laï JL; Andrieux J
Cancer Genet Cytogenet; 2004 Apr; 150(2):153-5. PubMed ID: 15066323
[TBL] [Abstract][Full Text] [Related]
12. Cohabiting t(12;22) and inv(3) primary rearrangements in an acute myelomonocytic leukemia (FAB M4) cell line.
MacLeod RA; Hu ZB; Kaufmann M; Drexler HG
Genes Chromosomes Cancer; 1996 Jun; 16(2):144-8. PubMed ID: 8818662
[TBL] [Abstract][Full Text] [Related]
13. Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia.
Park TS; Cheong JW; Song J; Choi JR
Leuk Res; 2009 Jul; 33(7):1001-4. PubMed ID: 19155067
[TBL] [Abstract][Full Text] [Related]
14. Therapy-related acute myelomonocytic leukemia following successful treatment for acute promyelocytic leukemia.
Todisco E; Testi AM; Avvisati G; Moleti ML; Cedrone M; Cimino G; Mancini F; Amadori S; Mandelli F
Leukemia; 1995 Sep; 9(9):1583-5. PubMed ID: 7658728
[TBL] [Abstract][Full Text] [Related]
15. Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
Zhang L; Alsabeh R; Mecucci C; La Starza R; Gorello P; Lee S; Lill M; Schreck R
Cancer Genet Cytogenet; 2007 Oct; 178(1):42-8. PubMed ID: 17889707
[TBL] [Abstract][Full Text] [Related]
16. Translocation between chromosome 5q35 and chromosome 11q13-- an unusual cytogenetic finding in a primary refractory acute myeloid leukemia.
Wang TF; Horsley SW; Lee KF; Chu SC; Li CC; Kao RH
Clin Lab Haematol; 2006 Jun; 28(3):160-3. PubMed ID: 16706931
[TBL] [Abstract][Full Text] [Related]
17. The chromosomal translocation (11;14) (p13; q11) in acute B-Cell lymphocytic leukemia.
Miao K; Li J; Qiu H; Zhang R; Chen L; Wu H; Wang R; Zhang J
Onkologie; 2010; 33(7):385-7. PubMed ID: 20631486
[TBL] [Abstract][Full Text] [Related]
18. [Double t (3; 21) in acute myelomonocytic leukemia transformed from chronic myelomonocytic leukemia].
Arai Y; Handa T; Nakamura F; Takahashi W; Maki K; Mitani K
Rinsho Ketsueki; 2002 Sep; 43(9):865-7. PubMed ID: 12412294
[TBL] [Abstract][Full Text] [Related]
19. Translocation (3;12)(q25;p11.2): a recurrent cytogenetic abnormality in acute myeloid leukemia.
Shah R; Rowland B; Richkind K; Mowery-Rushton P; Roherty S; Morgan R; Schlam M
Cancer Genet Cytogenet; 2005 Jan; 156(2):186-7. PubMed ID: 15642404
[No Abstract] [Full Text] [Related]
20. Therapy-related acute myeloid leukemia after successful therapy for acute promyelocytic leukemia with t(15;17): A case report and literature review.
Bao L; Lu X; Lai Y; Zhang X; Zhu H; Liu Y; Qin Y; Huang XJ
Leuk Res; 2009 Jul; 33(7):e64-8. PubMed ID: 19297021
[No Abstract] [Full Text] [Related]
[Next] [New Search]
