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International Journal of Pediatric Otorhinolaryngology|August 18, 2015
Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing lossDong-ye Chen, Wei-dong Zhu, Yong-chuan Chai, et al.
American Journal of Medical Genetics. Part A|September 25, 2014
Molecular etiology of non-dominant, non-syndromic, mild-to-moderate childhood hearing impairment in Chinese HansYongchuan Chai, Xiuhong Pang, Dongye Chen, et al.
The Annals of Otology, Rhinology, and Laryngology|April 19, 2015
A Novel Missense Mutation of NOG Interferes With the Dimerization of NOG and Causes Proximal Symphalangism Syndrome in a Chinese FamilyXiuhong Pang, Zhaoyan Wang, Yongchuan Chai, et al.
Frontiers in Cell and Developmental Biology|September 20, 2021
Single-Cell RNA Sequencing Analysis Reveals Greater Epithelial Ridge Cells Degeneration During Postnatal Development of Cochlea in RatsJianyong Chen, Dekun Gao, Junmin Chen, et al.
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