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5. Connexin-30 deletion analysis in connexin-26 heterozygotes. Stevenson VA; Ito M; Milunsky JM Genet Test; 2003; 7(2):151-4. PubMed ID: 12885339 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene]. Teriutin FM; Barashkov NA; Dzhemileva LU; Posukh OL; Fedotova EE; Gurinova EE; Fedorova SA; Tavartkiladze GA; Khusnutdinova EK Vestn Otorinolaringol; 2009; (2):17-9. PubMed ID: 19491791 [TBL] [Abstract][Full Text] [Related]
8. R75Q dominant mutation in GJB2 gene silenced by the in Cis recessive mutation c.35delG. Iossa S; Chinetti V; Corvino V; Marciano E; Franzè A Am J Med Genet A; 2010 Oct; 152A(10):2658-60. PubMed ID: 20815033 [No Abstract] [Full Text] [Related]
9. Epidemiological study of nonsyndromic hearing loss in Sicilian newborns. Niceta M; Fabiano C; Sammarco P; Piccione M; Antona V; Giuffrè M; Corsello G Am J Med Genet A; 2007 Jul; 143A(14):1666-70. PubMed ID: 17568408 [No Abstract] [Full Text] [Related]
10. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). Lench NJ; Markham AF; Mueller RF; Kelsell DP; Smith RJ; Willems PJ; Schatteman I; Capon H; Van De Heyning PJ; Van Camp G J Med Genet; 1998 Feb; 35(2):151-2. PubMed ID: 9507396 [TBL] [Abstract][Full Text] [Related]
11. A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family. Alemanno MS; Cama E; Santarelli R; Carella M; Zelante L; Toffolatti L; Palladino T; Melchionda S; Arslan E Int J Pediatr Otorhinolaryngol; 2009 Jan; 73(1):127-31. PubMed ID: 18990456 [TBL] [Abstract][Full Text] [Related]
12. Evaluation of childhood sensorineural hearing loss in the post-genome world. Lalwani AK Arch Otolaryngol Head Neck Surg; 2002 Jan; 128(1):88-9. PubMed ID: 11784265 [No Abstract] [Full Text] [Related]
13. The evaluation of children with sensorineural hearing loss. Greinwald JH; Hartnick CJ Arch Otolaryngol Head Neck Surg; 2002 Jan; 128(1):84-7. PubMed ID: 11784264 [No Abstract] [Full Text] [Related]
16. Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects. Neocleous V; Costi C; Shammas C; Spanou E; Anastasiadou V; Tanteles GA; Phylactou LA J Genet; 2014 Aug; 93(2):471-6. PubMed ID: 25189242 [No Abstract] [Full Text] [Related]
17. [Nonsyndromic sensorineural deafness--analysis of etiology in relatives]. Nowakowska-Szyrwinska E; Sobieszczanska-Radoszewska L Med Wieku Rozwoj; 2003; 7(1):21-5. PubMed ID: 13130165 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genetic analysis of the connexin-26 M34T variant. Griffith AJ J Med Genet; 2001 Jul; 38(7):E24. PubMed ID: 11432967 [No Abstract] [Full Text] [Related]
20. Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss. Bason L; Dudley T; Lewis K; Shah U; Potsic W; Ferraris A; Fortina P; Rappaport E; Krantz ID Clin Genet; 2002 Jun; 61(6):459-64. PubMed ID: 12121355 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]