Article
[The sequencing analyze of 915 newborn with GJB2 heterozygous mutation in Beijing].
Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery - 1 Jul 2015
Cui Qingjia, Huang Lihui, Ruan Yu, Du Yanshun, Zhao Liping, Yang Jun, Zhang Wei
Abstract excerpt
OBJECTIVE: To determine GJB2 allelic mutant and estimate probability of hereditary hearing loss in newborn with GJB2 heterozygous mutation in Beijing. METHOD: We performed genetic testing for sequencing of GJB2 gene for searching GJB2 allelic mutant in 915 newborn who received newborn deafness gene screening (GJB2 c. 235delC, GJB2 c. 299_300delAT, GJB2 c. 176191del16, GJB2 c. 35delG) in Beijing Tongren hospital,...
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