Author:
Wang Xudong,Hong Yongjun,Cai Peihong,Tang Ning,Chen Ying,Yan Tizhen,Liu Yinghua,Huang Qiuying,Li Qingge
Publisher
Springer Science and Business Media LLC
Reference33 articles.
1. Morton, N. Genetic epidemiology of hearing impairment. Annals of the New York Academy of Sciences 630, 16–31 (1991).
2. Guo, Y.F. et al. GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects. Acta oto-laryngologica 128, 297–303 (2008).
3. Lu, Y. et al. Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China. Journal of Biomedical Research 25, 309–318 (2011).
4. Duan, S.H., Zhu, Y.M., Wang, Y.L. & Guo, Y.F. Common molecular etiology of nonsyndromic hearing loss in 484 patients of 3 ethnicities in northwest China. Acta oto-laryngologica 135, 1–6 (2015).
5. Rabionet, R. & Estivill, X. Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) gene. Journal of medical genetics 36, 260–261 (1999).
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献