A Model of Waardenburg Syndrome Using Patient-Derived iPSCs With a SOX10 Mutation Displays Compromised Maturation and Function of the Neural Crest That Involves Inner Ear Developme...

by Jie Wen, Jie Wen, Jie Wen, Jian Song, Jian Song, Jian Song, Yijiang Bai, Yijiang Bai, Yijiang Bai, Yalan Liu, Yalan Liu, Yalan Liu, Xinzhang Cai, Xinzhang Cai, Xinzhang Cai, Lingyun Mei, Lingyun Mei, Lingyun Mei, Lu Ma, Chufeng He, Chufeng He, Chufeng He, Yong Feng, Yong Feng
Published 2021-08-01

New Genotypes and Phenotypes in Patients with 3 Subtypes of Waardenburg Syndrome Identified by Diagnostic Next-Generation Sequencing

by Wu Li, Lingyun Mei, Hongsheng Chen, Xinzhang Cai, Yalan Liu, Meichao Men, Xue Zhong Liu, Denise Yan, Jie Ling, Yong Feng
Published 2019-01-01

A New Genetic Diagnostic for Enlarged Vestibular Aqueduct Based on Next-Generation Sequencing.

by Yalan Liu, Lili Wang, Yong Feng, Chufeng He, Deyuan Liu, Xinzhang Cai, Lu Jiang, Hongsheng Chen, Chang Liu, Hong Wu, Lingyun Mei
Published 2016-01-01

A novel frameshift mutation of SMPX causes a rare form of X-linked nonsyndromic hearing loss in a Chinese family.

by Zhijie Niu, Yong Feng, Lingyun Mei, Jie Sun, Xueping Wang, Juncheng Wang, Zhengmao Hu, Yunpeng Dong, Hongsheng Chen, Chufeng He, Yalan Liu, Xinzhang Cai, Xuezhong Liu, Lu Jiang
Published 2017-01-01

Proband Whole-Exome Sequencing Identified Genes Responsible for Autosomal Recessive Non-Syndromic Hearing Loss in 33 Chinese Nuclear Families

by Shushan Sang, Shushan Sang, Jie Ling, Jie Ling, Jie Ling, Xuezhong Liu, Xuezhong Liu, Xuezhong Liu, Lingyun Mei, Lingyun Mei, Xinzhang Cai, Xinzhang Cai, Taoxi Li, Taoxi Li, Taoxi Li, Wu Li, Wu Li, Meng Li, Meng Li, Jie Wen, Jie Wen, Xianlin Liu, Xianlin Liu, Jing Liu, Jing Liu, Yalan Liu, Yalan Liu, Hongsheng Chen, Hongsheng Chen, Chufeng He, Chufeng He, Yong Feng, Yong Feng, Yong Feng, Yong Feng
Published 2019-07-01