【蔡承叡】評論
M5 t(9;11)(p21;q23) KMT2A/MLLT3M4 inv(16)(p13q22) CBFB/MYH11M3 t(15;17)(q24;q21) PML/RARAM2 t(8;21)(q22;q22) RUNX1/RUNX1T1
【etrnya】評論
the pericentric inversion of chromosome 16, inv(16)(p13;q22), or its variant t(16;16)(p13;q22). The chromosome 16 abnormalities, which are closely associated with the FAB subtype M4Eo, result in the creation of a fusion gene between the smooth muscle myosin-heavy chain gene (MYH11) at 16p13 and the core binding factor(CBF) gene at 16q22. The fusion protein product, CBF-MYH11, interacts with nuclear corepressors, leading to dysregulation of transcription...