DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Khandelwal G, Bhalla S, Khullar M, Panda NK.
High frequency of heterozygosity in GJB2 mutations among patients with non-syndromic hearing loss.
J Laryngol Otol 2009;
123 (03) 273-277
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