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25. 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]
26. Comprehensive interpretation of single-nucleotide substitutions in GJB2 reveals the genetic and phenotypic landscape of GJB2-related hearing loss. Xiang J; Sun X; Song N; Ramaswamy S; Abou Tayoun AN; Peng Z Hum Genet; 2023 Jan; 142(1):33-43. PubMed ID: 36048236 [TBL] [Abstract][Full Text] [Related]
27. Connexin mutation testing of children with nonsyndromic, autosomal recessive sensorineural hearing loss. Thomas MA; Der Kaloustian VM; Tewfik TL J Otolaryngol; 2004 Jun; 33(3):189-92. PubMed ID: 15841999 [TBL] [Abstract][Full Text] [Related]
28. Etiology of unilateral hearing loss in a national hereditary deafness repository. Dodson KM; Georgolios A; Barr N; Nguyen B; Sismanis A; Arnos KS; Norris VW; Chapman D; Nance WE; Pandya A Am J Otolaryngol; 2012; 33(5):590-4. PubMed ID: 22534022 [TBL] [Abstract][Full Text] [Related]
29. [Hearing loss associated with GJB2 gene mutation]. Cui Q; Huang L Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Oct; 27(19):1099-102. PubMed ID: 24417175 [TBL] [Abstract][Full Text] [Related]
30. The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar. Alkhidir S; El-Akouri K; Al-Dewik N; Khodjet-El-Khil H; Okashah S; Islam N; Ben-Omran T; Al-Shafai M Sci Rep; 2024 Feb; 14(1):4202. PubMed ID: 38378725 [TBL] [Abstract][Full Text] [Related]
31. Molecular epidemiology of DFNB1 deafness in France. Roux AF; Pallares-Ruiz N; Vielle A; Faugère V; Templin C; Leprevost D; Artières F; Lina G; Molinari N; Blanchet P; Mondain M; Claustres M BMC Med Genet; 2004 Mar; 5():5. PubMed ID: 15070423 [TBL] [Abstract][Full Text] [Related]
32. Systematic Review of Hearing Loss Genes in the African American Population. Worden CP; Jeyakumar A Otol Neurotol; 2019 Jun; 40(5):e488-e496. PubMed ID: 31083078 [TBL] [Abstract][Full Text] [Related]
33. Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort. Carvalho SDCES; Grangeiro CHP; Picanço-Albuquerque CG; Dos Anjos TO; De Molfetta GA; Silva WA; Ferraz VEF BMC Res Notes; 2018 Aug; 11(1):546. PubMed ID: 30068397 [TBL] [Abstract][Full Text] [Related]
34. Contribution of GJB2 mutations to hearing loss in the Hazara Division of Pakistan. Bukhari I; Mujtaba G; Naz S Biochem Genet; 2013 Aug; 51(7-8):524-9. PubMed ID: 23504403 [TBL] [Abstract][Full Text] [Related]
35. Auditory responses in cochlear implant users with and without GJB2 deafness. Propst EJ; Papsin BC; Stockley TL; Harrison RV; Gordon KA Laryngoscope; 2006 Feb; 116(2):317-27. PubMed ID: 16467727 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. 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]
39. [New recurrent extended deletion, including GJB2 and GJB6 genes, results in isolated sensorineural hearing impairment with autosomal recessive type of inheritance]. Bliznets EA; Makienko ON; Okuneva EG; Markova TG; Poliakov AV Genetika; 2014 Apr; 50(4):474-80. PubMed ID: 25715449 [TBL] [Abstract][Full Text] [Related]
40. GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review. Kenneson A; Van Naarden Braun K; Boyle C Genet Med; 2002; 4(4):258-74. PubMed ID: 12172392 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]