Author:
Zhao Minghong,Luo Xuemei,Zhao Qinfei,Yang Tong,Zhang Wenqian,Chen Zhigang,Zeng Shaoying,Chen Weifeng,Zhang Huijuan,Wang Qi,Wang Weihua,Zhang Xiaokang,Zhong Tianyu
Subject
Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health
Reference45 articles.
1. Concurrent hearing and genetic screening among newborns in Ningbo, China;Cao;Comput. Math. Methods Med.,2022
2. The importance of early genetic diagnostics of hearing loss in children;Božanić Urbančič;Medicina (Kaunas),2020
3. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China;Xiang;Int. J. Pediatr. Otorhinolaryngol.,2019
4. Genetic testing involving 100 common mutations for antenatal diagnosis of hereditary hearing loss in Chongqing, China;Hu;Medicine (Baltim.),2021
5. Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China;Zhang;Acta Otolaryngol.,2019