Precise Localization by Microdissection/Reverse ISH and FISH of the t(15;17)(q24;q21.1) Chromosomal Breakpoints Associated with Acute Promyelocytic Leukemia
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference31 articles.
1. 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukemia;Rowley;Lancet,1977
2. Molecular analysis of acute promyelocytic leukemia breakpoint cluster region on chromosome 17;Borrow;Science,1990
3. The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor α gene to a novel transcribed locus;de Thé;Nature,1990
4. The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR;de Thé;Cell,1991
5. Characterization of a zinc finger gene disrupted by the t(15;17) in acute promyelocytic leukemia;Goddard;Science,1991
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1. t(15;17)(q22;q21), t(15;17)(q22;q12), or t(15;17)(q24;q21)? A diagnostic entity in search of unanimity;Medical Oncology;2013-06-18
2. The first case of Philadelphia chromosome-negative acute promyelocytic leukemia following imatinib for chronic myelogenous leukemia;Cancer Genetics;2012-03
3. A report of three patients with an interstitial deletion of chromosome 15q24;American Journal of Medical Genetics Part A;2005
4. Molecular Cytogenetic Study of a Hemangiopericytoma in a Newborn;Cancer Genetics and Cytogenetics;2000-09
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