A case with a cytogenetically cryptic variant of the inv(16)(p13q22)/t(16;16)(p13;q22)
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference4 articles.
1. Acute myeloid leukaemia with recurrent genetic abnormalities;Arber,2008
2. Acute myeloid leukemia;Johansson,2009
3. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association;Le Beau;N Engl J Med,1983
4. CBFB/MYH11 fusion in a patient with AML-M4Eo and cytogenetically normal chromosomes 16;Pirc-Danoewinata;Genes Chromosomes Cancer,2000
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1. Integrative immunophenotypic and genetic characterization of acute myeloid leukemia with CBFB rearrangement;American Journal of Clinical Pathology;2024-05-27
2. Cryptic insertion of CBFB into MYH11 leading to a type D fusion in acute myeloid leukemia with normal karyotype;International Journal of Laboratory Hematology;2021-09-06
3. Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia;Medical Science Monitor;2016-08-26
4. Acute myeloid leukaemia (FAB AML-M4Eo) with cryptic insertion ofcbfbresulting incbfb-Myh11fusion;Hematological Oncology;2015-11-02
5. A novel cryptic insertion of CBFB into MYH11: importance of FISH probe design;Cancer Genetics;2014-10
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