165 related articles for article (PubMed ID: 17444514)
1. Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identification.
Tekin M; Arici ZS
Am J Med Genet A; 2007 Jul; 143A(14):1583-91. PubMed ID: 17444514
[TBL] [Abstract][Full Text] [Related]
2. Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey.
Duman D; Sirmaci A; Cengiz FB; Ozdag H; Tekin M
Genet Test Mol Biomarkers; 2011; 15(1-2):29-33. PubMed ID: 21117948
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.
Tamayo ML; Olarte M; Gelvez N; Gómez M; Frías JL; Bernal JE; Florez S; Medina D
Int J Pediatr Otorhinolaryngol; 2009 Jan; 73(1):97-101. PubMed ID: 19027181
[TBL] [Abstract][Full Text] [Related]
7. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene.
Denoyelle F; Weil D; Maw MA; Wilcox SA; Lench NJ; Allen-Powell DR; Osborn AH; Dahl HH; Middleton A; Houseman MJ; Dodé C; Marlin S; Boulila-ElGaïed A; Grati M; Ayadi H; BenArab S; Bitoun P; Lina-Granade G; Godet J; Mustapha M; Loiselet J; El-Zir E; Aubois A; Joannard A; Levilliers J; Garabédian EN; Mueller RF; Gardner RJ; Petit C
Hum Mol Genet; 1997 Nov; 6(12):2173-7. PubMed ID: 9336442
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients.
Bariş I; Kilinç MO; Tolun A
Clin Genet; 2001 Dec; 60(6):452-5. PubMed ID: 11846738
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The genetics of deafness.
Nance WE
Ment Retard Dev Disabil Res Rev; 2003; 9(2):109-19. PubMed ID: 12784229
[TBL] [Abstract][Full Text] [Related]
12. Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative mating.
Tekin M; Duman T; Boğoçlu G; Incesulu A; Comak E; Ilhan I; Akar N
Hum Mutat; 2003 May; 21(5):552-3. PubMed ID: 12673800
[TBL] [Abstract][Full Text] [Related]
13. Phenotype/genotype correlations in a DFNB1 cohort with ethnical diversity.
Angeli SI
Laryngoscope; 2008 Nov; 118(11):2014-23. PubMed ID: 18758381
[TBL] [Abstract][Full Text] [Related]
14. Role of DFNB1 mutations in hereditary hearing loss among assortative mating hearing impaired families from South India.
Amritkumar P; Jeffrey JM; Chandru J; Vanniya S P; Kalaimathi M; Ramakrishnan R; Karthikeyen NP; Srikumari Srisailapathy CR
BMC Med Genet; 2018 Jun; 19(1):105. PubMed ID: 29921236
[TBL] [Abstract][Full Text] [Related]
15. A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
Arnos KS; Welch KO; Tekin M; Norris VW; Blanton SH; Pandya A; Nance WE
Am J Hum Genet; 2008 Aug; 83(2):200-7. PubMed ID: 18656178
[TBL] [Abstract][Full Text] [Related]
16. GJB2 mutations are rare in probands with hearing loss in Chinese assortative mating families.
Chen G; Liu J; Dong J; Li J; Fu S
Int J Pediatr Otorhinolaryngol; 2014 Feb; 78(2):244-7. PubMed ID: 24359977
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. High incidence of profound deafness in an isolated community.
Zlotogora J; Barges S
Genet Test; 2003; 7(2):143-5. PubMed ID: 12885337
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. GJB2 gene mutations causing familial hereditary deafness in Turkey.
Bayazit YA; Cable BB; Cataloluk O; Kara C; Chamberlin P; Smith RJ; Kanlikama M; Ozer E; Cakmak EA; Mumbuc S; Arslan A
Int J Pediatr Otorhinolaryngol; 2003 Dec; 67(12):1331-5. PubMed ID: 14643477
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]