344 related articles for article (PubMed ID: 10983956)
1. Connexin26 mutations associated with nonsyndromic hearing loss.
Park HJ; Hahn SH; Chun YM; Park K; Kim HN
Laryngoscope; 2000 Sep; 110(9):1535-8. PubMed ID: 10983956
[TBL] [Abstract][Full Text] [Related]
2. Functional study of GJB2 in hereditary hearing loss.
Choung YH; Moon SK; Park HJ
Laryngoscope; 2002 Sep; 112(9):1667-71. PubMed ID: 12352684
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss.
Erbe CB; Harris KC; Runge-Samuelson CL; Flanary VA; Wackym PA
Laryngoscope; 2004 Apr; 114(4):607-11. PubMed ID: 15064611
[TBL] [Abstract][Full Text] [Related]
5. Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss.
Evirgen N; Solak M; Dereköy S; Erdoğan M; Yildiz H; Eser B; Arikan S; Erkoç A
Genet Test; 2008 Jun; 12(2):253-6. PubMed ID: 18554165
[TBL] [Abstract][Full Text] [Related]
6. Connexin26 gene ( GJB2): prevalence of mutations in the Chinese population.
Liu Y; Ke X; Qi Y; Li W; Zhu P
J Hum Genet; 2002; 47(12):688-90. PubMed ID: 12522692
[TBL] [Abstract][Full Text] [Related]
7. Cx26 gene mutations in idiopathic progressive hearing loss.
Ravecca F; Berrettini S; Forli F; Marcaccini M; Casani A; Baldinotti F; Fogli A; Siciliano G; Simi P
J Otolaryngol; 2005 Apr; 34(2):126-34. PubMed ID: 16076412
[TBL] [Abstract][Full Text] [Related]
8. GJB2 gene mutations in newborns with non-syndromic hearing impairment in Northern China.
Shi GZ; Gong LX; Xu XH; Nie WY; Lin Q; Qi YS
Hear Res; 2004 Nov; 197(1-2):19-23. PubMed ID: 15504600
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A novel connexin 26 compound heterozygous mutation results in deafness.
Harris KC; Erbe CB; Firszt JB; Flanary VA; Wackym PA
Laryngoscope; 2002 Jul; 112(7 Pt 1):1159-62. PubMed ID: 12169891
[TBL] [Abstract][Full Text] [Related]
11. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
Xiang YB; Tang SH; Li HZ; Xu CY; Chen C; Xu YZ; Ding LR; Xu XQ
Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():185-190. PubMed ID: 31035178
[TBL] [Abstract][Full Text] [Related]
12. Update of the spectrum of GJB2 mutations in 107 patients with nonsyndromic hearing loss in the Fujian population of China.
Chen T; Jiang L; Liu C; Shan H; Chen J; Yang B; Ou Q
Ann Hum Genet; 2014 May; 78(3):235-42. PubMed ID: 24645897
[TBL] [Abstract][Full Text] [Related]
13. A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews.
Lerer I; Sagi M; Ben-Neriah Z; Wang T; Levi H; Abeliovich D
Hum Mutat; 2001 Nov; 18(5):460. PubMed ID: 11668644
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.
Morell RJ; Kim HJ; Hood LJ; Goforth L; Friderici K; Fisher R; Van Camp G; Berlin CI; Oddoux C; Ostrer H; Keats B; Friedman TB
N Engl J Med; 1998 Nov; 339(21):1500-5. PubMed ID: 9819448
[TBL] [Abstract][Full Text] [Related]
16. Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
Abidi O; Boulouiz R; Nahili H; Bakhouch K; Wakrim L; Rouba H; Chafik A; Hassar M; Barakat A
Genet Test; 2008 Dec; 12(4):569-74. PubMed ID: 19072567
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss.
Jiang H; Chen J; Shan XJ; Li Y; He JG; Yang BB
Mol Med Rep; 2014 Jul; 10(1):379-86. PubMed ID: 24737404
[TBL] [Abstract][Full Text] [Related]
19. Unraveling the Diversity of GJB2 Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population.
El Fizazi K; Abbassi M; Nmer S; Laamarti H; ElAlami MN; Ouldim K; Bouguenouch L; Ridal M
Audiol Neurootol; 2024; 29(3):216-223. PubMed ID: 38253033
[TBL] [Abstract][Full Text] [Related]
20. Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario.
Maheshwari M; Vijaya R; Ghosh M; Shastri S; Kabra M; Menon PS
Am J Med Genet A; 2003 Jul; 120A(2):180-4. PubMed ID: 12833397
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
