Associated Papers
The prevalence of deafness-associated mutations in neonates: A meta-analysis of clinical trials.
Chen S et al.
International Journal of Pediatric Otorhinolaryngology, 2019
[An analysis of the mutation in GJB2，GJB3，SLC26A4 and mtDNA12SrRNA in new born].
Chai F et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery, 2017
Screening and analysis of mutation hot-spots in deafness-associated genes among adolescents with hearing loss.
Jiang H et al.
Molecular Medicine Reports, 2015
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