Report of a variant t(1;15;17)(p36;q22;q21.1) in a patient with acute promyelocytic leukemia
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference37 articles.
1. Fourth International Workshop on Chromosomes in Leukemia,1984
2. Evidence for a 15;17 translocation in every patient with acute promyelocytic leukemia;Larson;Am J Med,1984
3. A summary of cytogenetic morphologic and clinical data on t(8q−;21q+) and t(15q+;17q−) translocation leukemias in Japan;Sakurai;Cancer Genet Cytogenet,1982
4. Chromosome abnormalities in acute promyelocytic leukemia (APL);Van Den Berghe;Cancer,1979
5. 1517 translocation: a consistent chromosomal change in acute promyelocytic leukemia;Rowley;Lancet,1977
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1. A complex translocation (1;17;15) with spliced short‑type PML‑RARA fusion transcripts in acute promyelocytic leukemia: A case report;Experimental and Therapeutic Medicine;2018-12-13
2. The predictive value of morphological findings in early diagnosis of acute myeloid leukemia with recurrent cytogenetic abnormalities;Leukemia Research;2018-12
3. A complex translocation (3;17;15) in acute promyelocytic leukemia confirmed by fluorescence in situ hybridization;Oncology Letters;2016-10-18
4. Coexistence of t(15;17) and t(15;16;17) detected by fluorescence in situ hybridization in a patient with acute promyelocytic leukemia: A case report and literature review;Oncology Letters;2014-07-02
5. Acute promyelocytic leukemia with a novel variant (15;17) rearrangement;Journal of Hematopathology;2011-09-28
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