Delineation of translocation t(15; 17) in acute promyelocytic leukemia by chromosomal in situ suppression hybridization
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Oncology,Hematology
Reference33 articles.
1. Proposals for the classification of the acute leukaemias;Bennett;Br. J. Haemat.,1976
2. A variant form of hypergranular promyelocytic leukaemia (M3);Bennett;Br. J. Haemat.,1980
3. Acute promyelocytic leukemia;Groopman;Am. J. Hemat.,1979
4. Partial deletion of long arm of chromosome 17;Golomb,1976
5. 15/17 Translocation, a consistent chromosomal change in acute promyelocytic leukaemia;Rowley;Lancet,1977
Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Assessment of minimal residual disease in acute promyelocytic leukaemia with t(15;17) by chromosome painting;European Journal of Haematology;2009-04-24
2. Variant complex translocations involving chromosomes 1, 9, 9, 15 and 17 in acute promyelocytic leukemia without RARα/PML gene fusion rearrangement;Leukemia;1997-04
3. Fluorescence In situ Hybridization;Analytical Morphology;1996
4. Combined cytogenetic, FISH and molecular analysis in acute promyelocytic leukaemia at diagnosis and in complete remission;British Journal of Haematology;1995-12
5. Whole-Chromosome Hybridization;International Review of Cytology;1994
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