DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.
Absence of GJB6 mutations in Indian patients with non-syndromic hearing loss.
Int J Pediatr Otorhinolaryngol 2011;
75 (03) 356-359
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.