485 related articles for article (PubMed ID: 24529908)
1. Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran.
Bonyadi MJ; Fotouhi N; Esmaeili M
Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):637-40. PubMed ID: 24529908
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Frequency of GJB2 mutations, GJB6-D13S1830 and GJB6-D13S1854 deletions among patients with non-syndromic hearing loss from the central region of Iran.
Naddafnia H; Noormohammadi Z; Irani S; Salahshoorifar I
Mol Genet Genomic Med; 2019 Jul; 7(7):e00780. PubMed ID: 31162818
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.
Minárik G; Tretinárová D; Szemes T; Kádasi L
Int J Pediatr Otorhinolaryngol; 2012 Mar; 76(3):400-3. PubMed ID: 22281373
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients.
Dalamón V; Béhèran A; Diamante F; Pallares N; Diamante V; Elgoyhen AB
Hear Res; 2005 Sep; 207(1-2):43-9. PubMed ID: 15964725
[TBL] [Abstract][Full Text] [Related]
7. High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL).
Minárik G; Ferák V; Feráková E; Ficek A; Poláková H; Kádasi L
Gen Physiol Biophys; 2003 Dec; 22(4):549-56. PubMed ID: 15113126
[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. Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
Davarnia B; Babanejad M; Fattahi Z; Nikzat N; Bazazzadegan N; Pirzade A; Farajollahi R; Nishimura C; Jalalvand K; Arzhangi S; Kahrizi K; Smith RJ; Najmabadi H
Int J Pediatr Otorhinolaryngol; 2012 Feb; 76(2):268-71. PubMed ID: 22172221
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.
Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Reiisi S; Pourreza MR; Noori-Daloii MR; Tabatabaiefar MA
Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():121-126. PubMed ID: 29501291
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.
Kashef A; Nikzat N; Bazzazadegan N; Fattahi Z; Sabbagh-Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Najmabadi H; Kahrizi K
Int J Pediatr Otorhinolaryngol; 2015 Feb; 79(2):136-8. PubMed ID: 25555641
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico.
Hernández-Juárez AA; Lugo-Trampe Jde J; Campos-Acevedo LD; Lugo-Trampe A; Treviño-González JL; de-la-Cruz-Ávila I; Martínez-de-Villarreal LE
Int J Pediatr Otorhinolaryngol; 2014 Dec; 78(12):2107-12. PubMed ID: 25288386
[TBL] [Abstract][Full Text] [Related]
16. 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]
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 of IVS1+1G>A mutation among Iranian Azeri Turkish patients with autosomal recessive non-syndromic hearing loss (ARNSHL).
Bonyadi M; Fotouhi N; Esmaeili M
Int J Pediatr Otorhinolaryngol; 2011 Dec; 75(12):1612-5. PubMed ID: 22000900
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
Al-Achkar W; Al-Halabi B; Ali B; Moassass F
Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():82-87. PubMed ID: 28012540
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
