A cryptic three-way translocation involving chromosomes 8, 14, and 21 in a case of acute myeloid leukemia subtype M1
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology
Reference15 articles.
1. Morphologic characterization of acute myeloid leukemia with cytogenetic or molecular evidence of t(8;21), t(15;17), inv(16) and 11q23 abnormalities;Rozman;Haematologica,2002
2. 8;21 translocation in acute nonlymphocytic leukemia: occurrence in M1 and M2 FAB subtypes;Davey;Am J Clin Pathol,1989
3. Poor survival in t(8;21)(q22;q22)-associated acute myeloid leukaemia with leukocytosis;Billstrom;Eur J Haematol,1997
4. Acute myelogenous leukemia with an 8;21 translocation: a report on 148 cases from the Groupe Français de Cytogénétique Hématologique;Groupe Français de Cytogénétique Hématologique;Cancer Genet Cytogenet,1990
5. Translocation (8;21) and its variants in acute nonlymphocytic leukemia: the relative importance of chromosomes 8 and 21 to the genesis of the disease;Minamihisamatsu;Cancer Genet Cytogenet,1988
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1. Fusion Gene-Based Classification of Variant Cytogenetic Rearrangements in Acute Myeloid Leukemia;Genes;2023-02-03
2. Identification of a Cryptic t(8;20;21)(q22;p13;q22) Resulting in RUNX1T1/RUNX1 Fusion in a Patient with Newly Diagnosed Acute Myeloid Leukemia;Laboratory Medicine;2021-11-17
3. RUNX1 translocations and fusion genes in malignant hemopathies;Future Oncology;2011-01
4. Complex t(8;13;21)(q22;q14;q22)–A Novel Variant of t(8;21) in a Patient with Acute Myeloid Leukemia (AML–M2);Archives of Medical Research;2008-02
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