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2. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation. Xiao ZA; Xie DH Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707 [TBL] [Abstract][Full Text] [Related]
3. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. Rabionet R; Zelante L; López-Bigas N; D'Agruma L; Melchionda S; Restagno G; Arbonés ML; Gasparini P; Estivill X Hum Genet; 2000 Jan; 106(1):40-4. PubMed ID: 10982180 [TBL] [Abstract][Full Text] [Related]
4. The prevalence of connexin 26 ( GJB2) mutations in the Chinese population. Liu XZ; Xia XJ; Ke XM; Ouyang XM; Du LL; Liu YH; Angeli S; Telischi FF; Nance WE; Balkany T; Xu LR Hum Genet; 2002 Oct; 111(4-5):394-7. PubMed ID: 12384781 [TBL] [Abstract][Full Text] [Related]
5. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria]. Gallo-Terán J; Morales-Angulo C; del Castillo I; Villamar M; Moreno-Pelayo MA; García-Mantilla J; Moreno F Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196 [TBL] [Abstract][Full Text] [Related]
6. GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation. Ohtsuka A; Yuge I; Kimura S; Namba A; Abe S; Van Laer L; Van Camp G; Usami S Hum Genet; 2003 Apr; 112(4):329-33. PubMed ID: 12560944 [TBL] [Abstract][Full Text] [Related]
7. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families. Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379 [TBL] [Abstract][Full Text] [Related]
8. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation. Abidi O; Boulouiz R; Nahili H; Ridal M; Alami MN; Tlili A; Rouba H; Masmoudi S; Chafik A; Hassar M; Barakat A Int J Pediatr Otorhinolaryngol; 2007 Aug; 71(8):1239-45. PubMed ID: 17553572 [TBL] [Abstract][Full Text] [Related]
9. Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran. Bonyadi MJ; Fotouhi N; Esmaeili M Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):637-40. PubMed ID: 24529908 [TBL] [Abstract][Full Text] [Related]
10. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2. Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641 [TBL] [Abstract][Full Text] [Related]
11. Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene. Tekin M; Duman T; Boğoçlu G; Incesulu A; Cin S; Akar N Genet Couns; 2003; 14(4):379-86. PubMed ID: 14738110 [TBL] [Abstract][Full Text] [Related]
12. 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 [TBL] [Abstract][Full Text] [Related]
13. Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program. Propst EJ; Stockley TL; Gordon KA; Harrison RV; Papsin BC Int J Pediatr Otorhinolaryngol; 2006 Mar; 70(3):435-44. PubMed ID: 16125251 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574 [TBL] [Abstract][Full Text] [Related]
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18. Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population. Popova DP; Kaneva R; Varbanova S; Popov TM Eur Arch Otorhinolaryngol; 2012 Jun; 269(6):1589-92. PubMed ID: 22037723 [TBL] [Abstract][Full Text] [Related]
19. Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria. Janecke AR; Hirst-Stadlmann A; Günther B; Utermann B; Müller T; Löffler J; Utermann G; Nekahm-Heis D Hum Genet; 2002 Aug; 111(2):145-53. PubMed ID: 12189487 [TBL] [Abstract][Full Text] [Related]
20. Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK). Bousfiha A; Bakhchane A; Elrharchi S; Dehbi H; Kabine M; Nadifi S; Charoute H; Barakat A Curr Res Transl Med; 2016; 64(2):61-4. PubMed ID: 27316387 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]