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7. Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment. Santos RL; Wajid M; Pham TL; Hussan J; Ali G; Ahmad W; Leal SM Clin Genet; 2005 Jan; 67(1):61-8. PubMed ID: 15617550 [TBL] [Abstract][Full Text] [Related]
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