A novel mutation in POU3F4 in a Chinese family with X-linked non-syndromic hearing loss

por Huang, Bang-qing, Zeng, Jia-ling, Yuan, Yong-yi, Dai, Pu
Publicado 2015

Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

por Su, Yu, Gao, Xue, Huang, Sha-Sha, Mao, Jing-Ning, Huang, Bang-Qing, Zhao, Jian-Dong, Kang, Dong-Yang, Zhang, Xin, Dai, Pu
Publicado 2018

A gross deletion of the PAX3 gene in a large Chinese family with Waardenburg syndrome type I

por Yang, Shu-Zhi, Hou, Lei, Qi, Xin, Wang, Guo-Jian, Huang, Sha-Sha, Zhang, Shan-Shan, Huang, Bang-Qing, Yang, Ying, Li, Bei-Cheng, Liu, Shuo, Dai, Pu, Su, Yu
Publicado 2023