Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00283.x/fullpdf
Reference23 articles.
1. Statement of the American College of Medical Genetics on universal newborn hearing screening;Nance;Genet Med,2000
2. Genetic epidemiology of hearing impairment;Morton;Ann N Y Acad Sci,1991
3. Calvo J Rabionet R Gasparini P Estivill X Connexins and deafness homepage http://www.crg.es/deafness
4. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins;Rabionet;Hum Mutat,2000
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