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12. Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment. Loeza-Becerra F, Rivera-Vega Mdel R, Martínez-Saucedo M, Gonzalez-Huerta LM, Urueta-Cuellar H, Berrruecos-Villalobos P, Cuevas-Covarrubias S. Int J Pediatr Otorhinolaryngol; 2014 Jul; 78(7):1057-60. PubMed ID: 24774219 [Abstract] [Full Text] [Related]
13. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Batissoco AC, Abreu-Silva RS, Braga MC, Lezirovitz K, Della-Rosa V, Alfredo T, Otto PA, Mingroni-Netto RC. Ear Hear; 2009 Feb; 30(1):1-7. PubMed ID: 19125024 [Abstract] [Full Text] [Related]
14. Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment. Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M. Biochem Biophys Res Commun; 2009 Jul 31; 385(3):445-8. PubMed ID: 19465004 [Abstract] [Full Text] [Related]
15. 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 31; 77(5):714-6. PubMed ID: 23434199 [Abstract] [Full Text] [Related]
16. No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans. Wonkam A, Bosch J, Noubiap JJ, Lebeko K, Makubalo N, Dandara C. S Afr Med J; 2015 Jan 31; 105(1):23-6. PubMed ID: 26046157 [Abstract] [Full Text] [Related]