Acute promyelocytic leukemia with t(15;16;17;19) and unusual fluorescence in situ hybridization pattern with PML and RARA probes
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference30 articles.
1. 15;17 translocation, a consistent chromosomal change in acute promyelocytic leukemia;Rowley;Lancet,1977
2. The t(15;17) translocation in acute promyelocytic leukemia fuses retinoic acid receptor alpha gene to novel transcribed locus;deThe;Nature,1990
3. Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PML;Kakizuka;Cell,1991
4. Molecular analysis of acute promyelocytic leukemia, breakpoint cluster region on chromosome 17;Borrow;Science,1990
5. Acute promyelocytic leukemia;Warrell;N Engl J Med,1993
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2. 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 Genetics and Cytogenetics;2006-08
3. A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation;Cancer Genetics and Cytogenetics;2005-05
4. A New Complex Translocation (15;20;17)(q22;p13;q21) in Acute Promyelocytic Leukemia;Cancer Genetics and Cytogenetics;1998-03
5. Variant complex translocations involving chromosomes 1, 9, 9, 15 and 17 in acute promyelocytic leukemia without RARα/PML gene fusion rearrangement;Leukemia;1997-04
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