A rare case with typical acute promyelocytic leukemia morphology associated with isolated isochromosome 17q without RARα rearrangement
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology,General Medicine
Reference9 articles.
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2. Infantile acute promyelocytic leukemia without an RARα rearrangement;Hori;Pediatr Int,2011
3. Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA–PML fusion gene: report of 4 cases and review of the literature;Manola;Acta Haematol,2010
4. Acute promyelocytic leukemia with PML–RARA fusion on i(17q) and therapy-related acute myeloid leukemia;Lee;Cancer Genet Cytogenet,2005
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2. Acute promyelocytic leukemia with torque teno mini virus (TTMV)::RARAfusion: an approach to screening and diagnosis;2024-03-30
3. Cytogenetic profile and outcome of a pediatric acute promyelocytic leukemia patient presenting with isolated isochromosome 17q in absence of RARA rearrangement;Blood Cells, Molecules, and Diseases;2021-05
4. Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML and loss of one p53 gene: Report of two cases and literature review;Vojnosanitetski pregled;2019
5. The genetics and clinical characteristics of children morphologically diagnosed as acute promyelocytic leukemia;Leukemia;2018-12-21
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