These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
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]
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]
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]