404 related articles for article (PubMed ID: 14738110)
1. 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]
2. 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]
3. Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
Löffler J; Nekahm D; Hirst-Stadlmann A; Günther B; Menzel HJ; Utermann G; Janecke AR
Eur J Hum Genet; 2001 Mar; 9(3):226-30. PubMed ID: 11313763
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort.
Cama E; Melchionda S; Palladino T; Carella M; Santarelli R; Genovese E; Benettazzo F; Zelante L; Arslan E
Int J Audiol; 2009 Jan; 48(1):12-7. PubMed ID: 19173109
[TBL] [Abstract][Full Text] [Related]
6. The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness.
Petersen MB; Grigoriadou M; Koutroumpe M; Kokotas H
Int J Pediatr Otorhinolaryngol; 2012 Jul; 76(7):969-71. PubMed ID: 22484064
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. [Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria].
Gallo-Terán J; Morales-Angulo C; del Castillo I; Villamar M; Moreno-Pelayo MA; García-Mantilla J; Moreno F
Acta Otorrinolaringol Esp; 2002 Oct; 53(8):563-71. PubMed ID: 12530196
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations--phenotypic spectrum and frequencies of GJB2 mutations in Austria.
Janecke AR; Hirst-Stadlmann A; Günther B; Utermann B; Müller T; Löffler J; Utermann G; Nekahm-Heis D
Hum Genet; 2002 Aug; 111(2):145-53. PubMed ID: 12189487
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. [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]
16. 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]
17. Hearing loss associated with 35delG mutation in Connexin-26 (GJB2) gene: audiogram analysis.
Salvinelli F; Casale M; D'Ascanio L; Firrisi L; Greco F; Baldi A
J Laryngol Otol; 2004 Jan; 118(1):8-11. PubMed ID: 14979964
[TBL] [Abstract][Full Text] [Related]
18. A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
Cryns K; Orzan E; Murgia A; Huygen PL; Moreno F; del Castillo I; Chamberlin GP; Azaiez H; Prasad S; Cucci RA; Leonardi E; Snoeckx RL; Govaerts PJ; Van de Heyning PH; Van de Heyning CM; Smith RJ; Van Camp G
J Med Genet; 2004 Mar; 41(3):147-54. PubMed ID: 14985372
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]