DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Ramchander PV, Nandur VU, Dwarakanath K, Vishnupriya S, Padma T.
Prevalence of Cx26 (GJB2) gene mutations causing recessive nonsyndromic hearing impairment in India.
Int J Hum Genet 2005;
5 (04) 241-246
We do not assume any responsibility for the contents of the web pages of other providers.