Identification of a rare missense mutation in GJB1 and prenatal diagnosis in a Chinese family with CMT: A case report

por Huang, Xinyi, Wu, Xiaoli, Wu, Bei, Mou, Jing, Ma, Xingwei
Publicado 2022

A Three-Year Prospective Study Assessing the Application of Chromosomal Microarray Analysis in 576 High-Risk Pregnant Women

por Jiang, Minmin, Huang, Shengwen, Ma, Xingwei, Xie, Ping, Ren, Lingyan, Jin, Qian, Linghu, Keyan
Publicado 2022