Blood Research

Cytogenetic abnormalities and somatic mutations detected by MLPA (N=52).

13q14 deletion, N (%) 22 (42.3%)
Trisomy 12, N (%) 7 (13.4%)
11q (ATM) deletion, N (%) 5 (9.6%)
17p (TP53) deletion, N (%) 2 (3.8%)
No abnormality, N (%) 18 (34.6%)
Two abnormalities, N (%) 6 (11.5%)
NOTCH1 c.7541_7542delCT mutation 1 (1.9%)
MYD88 L265P mutation 0 (0.0%)
SF3B1 K700E mutation 0 (0.0%)
Blood Res 2020;55:131~138 https://doi.org/10.5045/br.2020.2020080
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