Characterization of cryptic rearrangements, deletion, complex variants of PML, RARA in acute promyelocytic leukemia
Author:
Publisher
CLOCKSS Archive
Subject
Genetics (clinical),Genetics
Cited by 5 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. Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention;Haematologica;2023-03-23
2. Typical, atypical and cryptic t(15;17)(q24;q21) ( PML::RARA ) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies;Genes, Chromosomes and Cancer;2022-06-10
3. Cytogenetics and FISH negative cryptic acute promyelocytic leukemia with CD56 expression;Indian Journal of Pathology and Microbiology;2021-04
4. Acute promyelocytic leukemia with a cryptic insertion of RARA into PML on chromosome 15 due to uniparental isodisomy: A case report;Oncology Letters;2017-04-03
5. Acute Promyelocytic Leukaemia: From a Specific Translocation to Cure by Targeted Therapies;Chromosomal Translocations and Genome Rearrangements in Cancer;2015
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