These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
246 related articles for article (PubMed ID: 15841999)
21. 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]
22. The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population. Sobe T; Vreugde S; Shahin H; Berlin M; Davis N; Kanaan M; Yaron Y; Orr-Urtreger A; Frydman M; Shohat M; Avraham KB Hum Genet; 2000 Jan; 106(1):50-7. PubMed ID: 10982182 [TBL] [Abstract][Full Text] [Related]
23. Autosomal recessive nonsyndromic deafness genes: a review. Duman D; Tekin M Front Biosci (Landmark Ed); 2012 Jun; 17(6):2213-36. PubMed ID: 22652773 [TBL] [Abstract][Full Text] [Related]
25. [Study of a mutation in connexin 26 gene associated with congenital sensorineural deafness]. Wang P; Wang Y; Liu X; Du B Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2001 Oct; 15(10):439-41. PubMed ID: 12541685 [TBL] [Abstract][Full Text] [Related]
31. De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss. Janecke AR; Nekahm D; Löffler J; Hirst-Stadlmann A; Müller T; Utermann G Hum Genet; 2001 Mar; 108(3):269-70. PubMed ID: 11354642 [TBL] [Abstract][Full Text] [Related]
32. A novel compound heterozygous mutation (35delG, 363delC) in the Connexin 26 gene causes non-syndromic autosomal recessive hearing loss. Onsori H; Rahmati M; Fazli D Acta Med Iran; 2014; 52(8):638-40. PubMed ID: 25149889 [TBL] [Abstract][Full Text] [Related]
33. 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]
34. Late postnatal onset of hearing loss due to GJB2 mutations. Pagarkar W; Bitner-Glindzicz M; Knight J; Sirimanna T Int J Pediatr Otorhinolaryngol; 2006 Jun; 70(6):1119-24. PubMed ID: 16469394 [TBL] [Abstract][Full Text] [Related]
35. Mutations in the connexin26/GJB2 gene are the most common event in non-syndromic hearing loss among the German population. Gabriel H; Kupsch P; Sudendey J; Winterhager E; Jahnke K; Lautermann J Hum Mutat; 2001 Jun; 17(6):521-2. PubMed ID: 11385713 [TBL] [Abstract][Full Text] [Related]
38. Temporal bone histopathology in connexin 26-related hearing loss. Jun AI; McGuirt WT; Hinojosa R; Green GE; Fischel-Ghodsian N; Smith RJ Laryngoscope; 2000 Feb; 110(2 Pt 1):269-75. PubMed ID: 10680928 [TBL] [Abstract][Full Text] [Related]
39. Advances in the Understanding of the Genetic Causes of Hearing Loss in Children Inform a Rational Approach to Evaluation. Carey JC; Palumbos JC Indian J Pediatr; 2016 Oct; 83(10):1150-6. PubMed ID: 26743077 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]