Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lancheng Huang"'
Autor:
Kai Zhou, Lancheng Huang, Menglong Feng, Xinlei Li, Yi Zhao, Fei Liu, Jiazhang Wei, Danxue Qin, Qiutian Lu, Min Shi, Shenhong Qu, Fengzhu Tang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Variants in the SLC26A4 gene are correlated with nonsyndromic hearing loss with an enlarged vestibular aqueduct (EVA). This study aimed to identify the genetic causes in a Chinese family with EVA, and the pathogenicity of the dete
Externí odkaz:
https://doaj.org/article/e8e1555c80df447dbcd2579ba1eb1af4
Autor:
Menglong, Feng, Kai, Zhou, Lancheng, Huang, Fengzhu, Tang, Shenhong, Qu, Qiutian, Lu, Ruichun, Chen, Fengti, Li
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(5)
To explore the genetic basis for a Chinese pedigree affected with non-syndromic hearing loss (NSHL).Commercialized gene chip was applied to detect common mutations associated with congenital deafness. Whole exome sequencing was carried out for patien
Autor:
Qiutian Lu, Yi Zhao, Fengzhu Tang, Min Shi, Menglong Feng, Shenhong Qu, Jiazhang Wei, Fei Liu, Dan-Xue Qin, Xinlei Li, Lancheng Huang, Kai Zhou
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Background Variants in the SLC26A4 gene are correlated with nonsyndromic hearing loss with an enlarged vestibular aqueduct (EVA). This study aimed to identify the genetic causes in a Chinese family with EVA, and the pathogenicity of the detected vari