310 related articles for article (PubMed ID: 21468573)
1. Mutations of the Connexin 26 gene in families with non-syndromic hearing loss.
Al-Achkar W; Moassass F; Al-Halabi B; Al-Ablog A
Mol Med Rep; 2011; 4(2):331-5. PubMed ID: 21468573
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Connexin 26 mutations and nonsyndromic hearing impairment in northern Finland.
Löppönen T; Väisänen ML; Luotonen M; Allinen M; Uusimaa J; Lindholm P; Mäki-Torkko E; Väyrynen M; Löppönen H; Leisti J
Laryngoscope; 2003 Oct; 113(10):1758-63. PubMed ID: 14520102
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss.
Evirgen N; Solak M; Dereköy S; Erdoğan M; Yildiz H; Eser B; Arikan S; Erkoç A
Genet Test; 2008 Jun; 12(2):253-6. PubMed ID: 18554165
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. High frequency of heterozygosity in GJB2 mutations among patients with non-syndromic hearing loss.
Khandelwal G; Bhalla S; Khullar M; Panda NK
J Laryngol Otol; 2009 Mar; 123(3):273-7. PubMed ID: 18570691
[TBL] [Abstract][Full Text] [Related]
10. Cx26 gene mutations in idiopathic progressive hearing loss.
Ravecca F; Berrettini S; Forli F; Marcaccini M; Casani A; Baldinotti F; Fogli A; Siciliano G; Simi P
J Otolaryngol; 2005 Apr; 34(2):126-34. PubMed ID: 16076412
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. 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]
14. 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]
15. Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene.
Tekin M; Duman T; Boğoçlu G; Incesulu A; Cin S; Akar N
Genet Couns; 2003; 14(4):379-86. PubMed ID: 14738110
[TBL] [Abstract][Full Text] [Related]
16. 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]
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. Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL).
Mishra S; Pandey H; Srivastava P; Mandal K; Phadke SR
Indian J Pediatr; 2018 Dec; 85(12):1061-1066. PubMed ID: 29542069
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
