2.
90例CBF-AML患儿常见细胞遗传学特征 [例(%)]
| 项目 | CBFB-MYH11组(n=16) | AML1-ETO组(n=74) |
| 性染色体缺失 | ||
| -X | 0(0) | 10(14) |
| -Y | 1(6) | 17(23) |
| 染色体缺失 | ||
| -5 | 0(0) | 2(2) |
| 7q- | 0(0) | 1(1) |
| -9/9q- | 0(0) | 4(5) |
| 17q- | 0(0) | 2(2) |
| 染色体三体 | ||
| +4 | 1(6) | 2(2) |
| +8 | 1(6) | 0(0) |
| +22 | 3(18) | 0(0) |
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