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.
266 related articles for article (PubMed ID: 11698809)
1. GJB2 (connexin 26) mutations and childhood deafness in Thailand. Kudo T; Ikeda K; Oshima T; Kure S; Tammasaeng M; Prasansuk S; Matsubara Y Otol Neurotol; 2001 Nov; 22(6):858-61. PubMed ID: 11698809 [TBL] [Abstract][Full Text] [Related]
2. Mutation spectrum of the connexin 26 (GJB2) gene in Taiwanese patients with prelingual deafness. Hwa HL; Ko TM; Hsu CJ; Huang CH; Chiang YL; Oong JL; Chen CC; Hsu CK Genet Med; 2003; 5(3):161-5. PubMed ID: 12792423 [TBL] [Abstract][Full Text] [Related]
3. Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population. Kudo T; Ikeda K; Kure S; Matsubara Y; Oshima T; Watanabe Ki; Kawase T; Narisawa K; Takasaka T Am J Med Genet; 2000 Jan; 90(2):141-5. PubMed ID: 10607953 [TBL] [Abstract][Full Text] [Related]
4. Identification of 605ins46, a novel GJB2 mutation in a Japanese family. Yuge I; Ohtsuka A; Matsunaga T; Usami S Auris Nasus Larynx; 2002 Oct; 29(4):379-82. PubMed ID: 12393046 [TBL] [Abstract][Full Text] [Related]
5. Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan. Wang YC; Kung CY; Su MC; Su CC; Hsu HM; Tsai CC; Lin CC; Li SY Eur J Hum Genet; 2002 Aug; 10(8):495-8. PubMed ID: 12111646 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations. Sugata A; Fukushima K; Sugata K; Fukuda S; Kimura N; Gunduz M; Kasai N; Usami S; Smith RJ; Nishizaki K Auris Nasus Larynx; 2002 Jul; 29(3):231-9. PubMed ID: 12167443 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Prevalence of GJB2 mutations in prelingual deafness in the Greek population. Pampanos A; Economides J; Iliadou V; Neou P; Leotsakos P; Voyiatzis N; Eleftheriades N; Tsakanikos M; Antoniadi T; Hatzaki A; Konstantopoulou I; Yannoukakos D; Gronskov K; Brondum-Nielsen K; Grigoriadou M; Gyftodimou J; Iliades T; Skevas A; Petersen MB Int J Pediatr Otorhinolaryngol; 2002 Sep; 65(2):101-8. PubMed ID: 12176179 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation. Ohtsuka A; Yuge I; Kimura S; Namba A; Abe S; Van Laer L; Van Camp G; Usami S Hum Genet; 2003 Apr; 112(4):329-33. PubMed ID: 12560944 [TBL] [Abstract][Full Text] [Related]
13. 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]
15. Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians. Yan D; Park HJ; Ouyang XM; Pandya A; Doi K; Erdenetungalag R; Du LL; Matsushiro N; Nance WE; Griffith AJ; Liu XZ Hum Genet; 2003 Dec; 114(1):44-50. PubMed ID: 14505035 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. [High prevalence of connexin-26 (GJB2) mutation in cochlear implant recipients]. Chen DY; Chen XW; Cao KL; Jin X; Zuo J; Wei CG; Fang FD Zhonghua Yi Xue Za Zhi; 2006 Nov; 86(44):3114-7. PubMed ID: 17313762 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. [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] [Next] [New Search]