A new variant translocation 11;17 in a patient with acute promyelocytic leukemia together with t(7;12)
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference24 articles.
1. Further evidence for a non-random chromosomal abnormality in acute promyelocytic leukemia;Rowley;Int J Cancer,1977
2. Chromosomes in acute promyelocytic leukemia,1984
3. Report of the committee on structural chromosome changes in neoplasia;Bloomfield,1987
4. Evidence for a 15;17 translocation in every patient with acute promyelocytic leukemia;Larson;Am J Med,1984
5. The occurrence of translocation (15;17) in acute promyelocytic leukemia: An update;De Braekeleer;Cancer Genet Cytogenet,1986
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1. Cryptic t(15;17) acute promyelocytic leukemia with a karyotype of add(11)(p15) and t(13,20)- A case report with a literature review;Bosnian Journal of Basic Medical Sciences;2020-10-09
2. RARAfusion genes in acute promyelocytic leukemia: a review;Expert Review of Hematology;2014-04-10
3. Histone Acetylation Modifiers in the Pathogenesis of Malignant Disease;Molecular Medicine;2000-08
4. A New Variant Translocation of t(15;17) in a Patient with Acute Promyelocytic Leukemia (M3): t(15;19;17)(q22;p13;q12);Cancer Genetics and Cytogenetics;1998-04
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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