A novel mutation of the PAX3 gene in a Chinese family with Waardenburg syndrome type I

por Ma, Jing, Lin, Ken, Jiang, Hong‐chao, Yang, Yanli, Zhang, Yu, Yang, Guilian, Sun, Hao, Ming, Cheng, Bi, Xianyun, Zhang, Tiesong, Ruan, Biao
Publicado 2019

Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel

por Ma, Jing, Ma, Xiuli, Lin, Ken, Huang, Rui, Bi, Xianyun, Ming, Cheng, Li, Li, Li, Xia, Li, Guo, Zhao, Liping, Yang, Tao, Gao, Yingqin, Zhang, Tiesong
Publicado 2023