1083 related articles for article (PubMed ID: 10376574)
1. 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]
2. 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]
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. Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
Prasad S; Cucci RA; Green GE; Smith RJ
Hum Mutat; 2000 Dec; 16(6):502-8. PubMed ID: 11102979
[TBL] [Abstract][Full Text] [Related]
5. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
Schade G; Kothe C; Ruge G; Hess M; Meyer CG
Laryngorhinootologie; 2003 Jun; 82(6):397-401. PubMed ID: 12851846
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. GJB2: the spectrum of deafness-causing allele variants and their phenotype.
Azaiez H; Chamberlin GP; Fischer SM; Welp CL; Prasad SD; Taggart RT; del Castillo I; Van Camp G; Smith RJ
Hum Mutat; 2004 Oct; 24(4):305-11. PubMed ID: 15365987
[TBL] [Abstract][Full Text] [Related]
9. Prevalence of 35delG/GJB2 and del (GJB6-D13S1830) mutations in patients with non-syndromic deafness from a population of Espírito Santo-Brazil.
Cordeiro-Silva Mde F; Barbosa A; Santiago M; Provetti M; Rabbi-Bortolini E
Braz J Otorhinolaryngol; 2010; 76(4):428-32. PubMed ID: 20835527
[TBL] [Abstract][Full Text] [Related]
10. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
Trabelsi M; Bahri W; Habibi M; Zainine R; Maazoul F; Ghazi B; Chaabouni H; Mrad R
Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population.
Popova DP; Kaneva R; Varbanova S; Popov TM
Eur Arch Otorhinolaryngol; 2012 Jun; 269(6):1589-92. PubMed ID: 22037723
[TBL] [Abstract][Full Text] [Related]
14. Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcome.
Riahi Z; Zainine R; Mellouli Y; Hannachi R; Bouyacoub Y; Laroussi N; Beltaief N; Kefi R; Romdhane L; Bonnet C; Abdelhak S; Besbes G
Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1481-4. PubMed ID: 23856378
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
Norris VW; Arnos KS; Hanks WD; Xia X; Nance WE; Pandya A
Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
[TBL] [Abstract][Full Text] [Related]
17. Performance of cochlear implant recipients with GJB2-related deafness.
Green GE; Scott DA; McDonald JM; Teagle HF; Tomblin BJ; Spencer LJ; Woodworth GG; Knutson JF; Gantz BJ; Sheffield VC; Smith RJ
Am J Med Genet; 2002 May; 109(3):167-70. PubMed ID: 11977173
[TBL] [Abstract][Full Text] [Related]
18. Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.
Iliades T; Eleftheriades N; Iliadou V; Pampanos A; Voyiatzis N; Economides J; Leotsakos P; Neou P; Tsakanikos M; Antoniadi T; Konstantopoulou I; Yannoukakos D; Grigoriadou M; Skevas A; Petersen MB
ORL J Otorhinolaryngol Relat Spec; 2002; 64(5):321-3. PubMed ID: 12417772
[TBL] [Abstract][Full Text] [Related]
19. Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.
Teek R; Kruustük K; Zordania R; Joost K; Reimand T; Möls T; Oitmaa E; Kahre T; Tõnisson N; Ounap K
Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1007-12. PubMed ID: 20708129
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
