Acute myeloid leukemia with inv(16)(p13.1q22) and deletion of the 5 ’MYH11/3’CBFB gene fusion: a report of two cases and literature review

Abnormalities of chromosome 16 are found in about 5 –8% of acute myeloid leukemia (AML). The AML with inv(16)(p13.1q22) or t (16;16)(p13.1;q22) is associated with a high rate of complete remission (CR) and favo...

Source: Molecular Cytogenetics - January 30, 2020 Category: Molecular Biology Authors: Lili Lv, Jingwei Yu and Zhongxia Qi Tags: Case Report Source Type: research