Complex rearrangement in acute myeloid leukemia M2 with RUNX1/RUNX1T1 fusion involving chromosomes 8, 17 and 21

Abstract Background The translocation t(8;21)(q22;q22) is one of the most frequent chromosomal abnormalities associated with acute myeloid leukemia (AML) sub type M2. About 3–5 % of cases with additional chromosomal abnormalities, including structural and numerical ones, are reported to include a co...

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Главные авторы:	Shiba Ranjan Mishra, Leena Rawal, Moneeb A. K. Othman, Atul Thatai, Aditi Sarkar, Vandana Lal, Saurabh Kumar Bhattacharya
Формат:	Artigo
Язык:	Inglês
Опубликовано:	BMC 2021-05-01
Серии:	Molecular Cytogenetics
Предметы:	Variant translocation t(8;21) Acute myeloid leukemia Molecular cytogenetics
Online-ссылка:	https://doi.org/10.1186/s13039-021-00541-6
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