Postnatal Development of Microglia-Like Cells in Mouse Cochlea

by Penghui Chen, Yongchuan Chai, Haijin Liu, Gen Li, Longhao Wang, Tao Yang, Hao Wu
Published 2018-01-01

Characterization of spectrum, de novo rate and genotype-phenotype correlation of dominant GJB2 mutations in Chinese hans.

by Xiuhong Pang, Yongchuan Chai, Lianhua Sun, Dongye Chen, Ying Chen, Zhihua Zhang, Hao Wu, Tao Yang
Published 2014-01-01

A 1.6-Mb microdeletion in chromosome 17q22 leads to NOG-related symphalangism spectrum disorder without intellectual disability.

by Xiuhong Pang, Huajie Luo, Yongchuan Chai, Xiaowen Wang, Lianhua Sun, Longxia He, Penghui Chen, Hao Wu, Tao Yang
Published 2015-01-01

Identification and Characterization of a Cryptic Genomic Deletion-Insertion in EYA1 Associated with Branchio-Otic Syndrome

by Hao Zheng, Jun Xu, Yu Wang, Yun Lin, Qingqiang Hu, Xing Li, Jiusheng Chu, Changling Sun, Yongchuan Chai, Xiuhong Pang
Published 2021-01-01

Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss.

by Ying Chen, Zhentao Wang, Zhaoyan Wang, Dongye Chen, Yongchuan Chai, Xiuhong Pang, Lianhua Sun, Xiaowen Wang, Tao Yang, Hao Wu
Published 2015-01-01

The p.V37I exclusive genotype of GJB2: a genetic risk-indicator of postnatal permanent childhood hearing impairment.

by Lei Li, Jingrong Lu, Zheng Tao, Qi Huang, Yongchuan Chai, Xiaohua Li, Zhiwu Huang, Yun Li, Mingliang Xiang, Jun Yang, Guoyin Yao, Yu Wang, Tao Yang, Hao Wu
Published 2012-01-01

Association of GRM7 variants with different phenotype patterns of age-related hearing impairment in an elderly male Han Chinese population.

by Huajie Luo, Tao Yang, Xiaojie Jin, Xiuhong Pang, Jiping Li, Yongchuan Chai, Lei Li, Yi Zhang, Luping Zhang, Zhihua Zhang, Wenjing Wu, Qin Zhang, Xianting Hu, Jingwen Sun, Xuemei Jiang, Zhuping Fan, Zhiwu Huang, Hao Wu
Published 2013-01-01