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42. High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India. Joseph AY; Rasool TJ Int J Pediatr Otorhinolaryngol; 2009 Mar; 73(3):437-43. PubMed ID: 19157576 [TBL] [Abstract][Full Text] [Related]
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45. Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identification. Tekin M; Arici ZS Am J Med Genet A; 2007 Jul; 143A(14):1583-91. PubMed ID: 17444514 [TBL] [Abstract][Full Text] [Related]
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48. [The principles of molecular diagnosis of recessive forms of prelingual non-syndromic hearing loss]. Wiszniewska J; Wiszniewski W; Bal J Med Wieku Rozwoj; 2002; 6(4):309-18. PubMed ID: 12810983 [TBL] [Abstract][Full Text] [Related]
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53. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness. Trabelsi M; Bahri W; Habibi M; Zainine R; Maazoul F; Ghazi B; Chaabouni H; Mrad R Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199 [TBL] [Abstract][Full Text] [Related]
54. Prevalence of GJB2 mutations in prelingual deafness in the Greek population. Pampanos A; Economides J; Iliadou V; Neou P; Leotsakos P; Voyiatzis N; Eleftheriades N; Tsakanikos M; Antoniadi T; Hatzaki A; Konstantopoulou I; Yannoukakos D; Gronskov K; Brondum-Nielsen K; Grigoriadou M; Gyftodimou J; Iliades T; Skevas A; Petersen MB Int J Pediatr Otorhinolaryngol; 2002 Sep; 65(2):101-8. PubMed ID: 12176179 [TBL] [Abstract][Full Text] [Related]
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58. Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness. Lezirovitz K; Pardono E; de Mello Auricchio MT; de Carvalho E Silva FL; Lopes JJ; Abreu-Silva RS; Romanos J; Batissoco AC; Mingroni-Netto RC Eur J Hum Genet; 2008 Jan; 16(1):89-96. PubMed ID: 17851452 [TBL] [Abstract][Full Text] [Related]
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