651 related articles for article (PubMed ID: 12384781)
1. 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]
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. 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]
4. 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]
5. 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]
6. 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]
7. Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
Pandya A; Arnos KS; Xia XJ; Welch KO; Blanton SH; Friedman TB; Garcia Sanchez G; Liu MD XZ; Morell R; Nance WE
Genet Med; 2003; 5(4):295-303. PubMed ID: 12865758
[TBL] [Abstract][Full Text] [Related]
8. Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness.
Cordeiro-Silva Mde F; Barbosa A; Santiago M; Provetti M; Dettogni RS; Tovar TT; Rabbi-Bortolini E; Louro ID
Mol Biol Rep; 2011 Feb; 38(2):1309-13. PubMed ID: 20563649
[TBL] [Abstract][Full Text] [Related]
9. Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.
Shahin H; Walsh T; Sobe T; Lynch E; King MC; Avraham KB; Kanaan M
Hum Genet; 2002 Mar; 110(3):284-9. PubMed ID: 11935342
[TBL] [Abstract][Full Text] [Related]
10. Connexin-26 mutations in sporadic and inherited sensorineural deafness.
Estivill X; Fortina P; Surrey S; Rabionet R; Melchionda S; D'Agruma L; Mansfield E; Rappaport E; Govea N; Milà M; Zelante L; Gasparini P
Lancet; 1998 Feb; 351(9100):394-8. PubMed ID: 9482292
[TBL] [Abstract][Full Text] [Related]
11. [Prevalence of GJB2 mutations in Uigur and Han ethnic populations with deafness in Xinjiang region of China].
Li Q; Dai P; Huang DL; Zhang J; Wang GJ; Zhu QW; Liu X; Han DY
Zhonghua Yi Xue Za Zhi; 2007 Nov; 87(42):2977-81. PubMed ID: 18261328
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The prevalence of the 235delC GJB2 mutation in a Chinese deaf population.
Dai P; Yu F; Han B; Yuan Y; Li Q; Wang G; Liu X; He J; Huang D; Kang D; Zhang X; Yuan H; Schmitt E; Han D; Wong LJ
Genet Med; 2007 May; 9(5):283-9. PubMed ID: 17505205
[TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of familial GJB2-related deafness in Iranian Azeri Turkish patients.
Bonyadi M; Esmaeili M; Abhari M; Lotfi A
Genet Test Mol Biomarkers; 2009 Oct; 13(5):689-92. PubMed ID: 19715472
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness.
Belintani Piatto V; Maria Goloni Bertollo E; Lúcia Sartorato E; Victor Maniglia J
Hear Res; 2004 Oct; 196(1-2):87-93. PubMed ID: 15464305
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions.
Talbi S; Bonnet C; Boudjenah F; Mansouri MT; Petit C; Ammar Khodja F
Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():157-160. PubMed ID: 31200317
[TBL] [Abstract][Full Text] [Related]
18. Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant.
Gazzaz B; Weil D; Raïs L; Akhyat O; Azeddoug H; Nadifi S
Hear Res; 2005 Dec; 210(1-2):80-4. PubMed ID: 16243461
[TBL] [Abstract][Full Text] [Related]
19. Connexin 26 (GJB2) gene mutations linked with autosomal recessive non-syndromic sensor neural hearing loss in the Iraqi population.
Al-Janabi AM; Ahmmed HS; Al-Khafaji SM
J Med Life; 2021; 14(6):841-846. PubMed ID: 35126756
[TBL] [Abstract][Full Text] [Related]
20. GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.
Tekin M; Xia XJ; Erdenetungalag R; Cengiz FB; White TW; Radnaabazar J; Dangaasuren B; Tastan H; Nance WE; Pandya A
Ann Hum Genet; 2010 Mar; 74(2):155-64. PubMed ID: 20201936
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
