Long-term Outcomes of Bone Conduction Hearing Implants in Patients With Bilateral Microtia-atresia

por Fan, Xinmiao, Yang, Tengyu, Niu, Xiaomin, Wang, Yibei, Fan, Yue, Chen, Xiaowei
Publicado 2019

Altered regional activity and connectivity of functional brain networks in congenital unilateral conductive hearing loss

por Yang, Tengyu, Liu, Qiang, Fan, Xinmiao, Hou, Bo, Wang, Jian, Chen, Xiaowei
Publicado 2021

Target sequencing of 307 deafness genes identifies candidate genes implicated in microtia

por Wang, Pu, Fan, Xinmiao, Wang, Yibei, Fan, Yue, Liu, Yaping, Zhang, Shuyang, Chen, Xiaowei
Publicado 2017

TCOF1 pathogenic variants identified by Whole-exome sequencing in Chinese Treacher Collins syndrome families and hearing rehabilitation effect

por Fan, Xinmiao, Wang, Yibei, Fan, Yue, Du, Huiqian, Luo, Nana, Zhang, Shuyang, Chen, Xiaowei
Publicado 2019

Identification of sequence variants associated with severe microtia-astresia by targeted sequencing

por Wang, Pu, Wang, Yibei, Fan, Xinmiao, Liu, Yaping, Fan, Yue, Liu, Tao, Chen, Chongjian, Zhang, Shuyang, Chen, Xiaowei
Publicado 2019

Whole-Exome Sequencing of Discordant Monozygotic Twin Families for Identification of Candidate Genes for Microtia-Atresia

por Fan, Xinmiao, Ping, Lu, Sun, Hao, Chen, Yushan, Wang, Pu, Liu, Tao, Jiang, Rui, Zhang, Xuegong, Chen, Xiaowei
Publicado 2020

A Mutation in VWA1, Encoding von Willebrand Factor A Domain-Containing Protein 1, Is Associated With Hemifacial Microsomia

por Wang, Yibei, Ping, Lu, Luan, Xiaodong, Chen, Yushan, Fan, Xinmiao, Li, Lianyan, Liu, Yaping, Wang, Pu, Zhang, Shuyang, Zhang, Bo, Chen, Xiaowei
Publicado 2020