Case Report: Prenatal diagnosis of a rare complex fetal karyotype 47,U,t(10;13)(p15;q22)mat,+der(13)t(10;13)dmat resulting from 3:1 meiotic segregation of a maternal balanced translocation
病例报告:产前诊断一例罕见的复杂胎儿核型 47,U,t(10;13)(p15;q22)mat,+der(13)t(10;13)dmat,该核型由母源平衡易位在减数分裂中以 3:1 的比例分离所致。
期刊:Frontiers in Reproductive Health
影响因子:2.9
doi:10.3389/frph.2025.1737392
Deng, G S; Zhang, D H; Lai, Y Q; Song, J J; Pan, J J; Liang, X F; Lu, Y H; Ning, S S; Li, W C; Li, X; Chen, Y Y; Li, D R; Li, L L; Liang, Y N