Associated Papers
Genetics Landscape of Nonsyndromic Hearing Loss in Indian Populations.
Ray M et al.
Journal of Pediatric Genetics, 2022
Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identification.
Tekin M et al.
American Journal of Medical Genetics. Part A, 2007
Contribution of connexin26 (GJB2) mutations and founder effect to non-syndromic hearing loss in India.
RamShankar M et al.
Journal of Medical Genetics, 2003
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