141 related articles for article (PubMed ID: 11494963)
1. Recurrent mutations in the deafness gene GJB2 (connexin 26) in British Asian families.
Rickard S; Kelsell DP; Sirimana T; Rajput K; MacArdle B; Bitner-Glindzicz M
J Med Genet; 2001 Aug; 38(8):530-3. PubMed ID: 11494963
[No Abstract] [Full Text] [Related]
2. [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].
Birkenhäger R; Zimmer AJ; Maier W; Schipper J
Laryngorhinootologie; 2006 Mar; 85(3):191-6. PubMed ID: 16547895
[TBL] [Abstract][Full Text] [Related]
3. [Nonsyndromic sensorineural deafness--analysis of etiology in relatives].
Nowakowska-Szyrwinska E; Sobieszczanska-Radoszewska L
Med Wieku Rozwoj; 2003; 7(1):21-5. PubMed ID: 13130165
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects.
Neocleous V; Costi C; Shammas C; Spanou E; Anastasiadou V; Tanteles GA; Phylactou LA
J Genet; 2014 Aug; 93(2):471-6. PubMed ID: 25189242
[No Abstract] [Full Text] [Related]
6. 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]
7. [Cochlear implantation in a child with congenital sensorineural deafness due to 35 DELG mutation in GJB2 (connexin 26) gene].
Teriutin FM; Barashkov NA; Dzhemileva LU; Posukh OL; Fedotova EE; Gurinova EE; Fedorova SA; Tavartkiladze GA; Khusnutdinova EK
Vestn Otorinolaringol; 2009; (2):17-9. PubMed ID: 19491791
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India.
Joseph AY; Rasool TJ
Int J Pediatr Otorhinolaryngol; 2009 Mar; 73(3):437-43. PubMed ID: 19157576
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. GJB2 (connexin 26) mutations and childhood deafness in Thailand.
Kudo T; Ikeda K; Oshima T; Kure S; Tammasaeng M; Prasansuk S; Matsubara Y
Otol Neurotol; 2001 Nov; 22(6):858-61. PubMed ID: 11698809
[TBL] [Abstract][Full Text] [Related]
12. Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss.
Yoong SY; Mavrogiannis LA; Wright J; Fairley L; Bennett CP; Charlton RS; Spencer N
Arch Dis Child; 2011 Sep; 96(9):798-803. PubMed ID: 21586435
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. [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]
15. Novel mutations in the connexin 26 gene (GJB2) responsible for childhood deafness in the Japanese population.
Kudo T; Ikeda K; Kure S; Matsubara Y; Oshima T; Watanabe Ki; Kawase T; Narisawa K; Takasaka T
Am J Med Genet; 2000 Jan; 90(2):141-5. PubMed ID: 10607953
[TBL] [Abstract][Full Text] [Related]
16. Absence of deafness-associated connexin-26 (GJB2) gene mutations in the Omani population.
Simsek M; Al-Wardy N; Al-Khayat A; Shanmugakonar M; Al-Bulushi T; Al-Khabory M; Al-Mujeni S; Al-Harthi S
Hum Mutat; 2001 Dec; 18(6):545-6. PubMed ID: 11748849
[TBL] [Abstract][Full Text] [Related]
17. Rapid detection of the 35delG mutation in the GJB2 gene in childhood deafness.
Tessa A; Patrono C; Santorelli FM; Giannotti A; Digilio MC; Pacifico C; Presuttari F; Tieri L
J Med Screen; 2000; 7(3):167. PubMed ID: 11126168
[No Abstract] [Full Text] [Related]
18. An unusual mucocutaneous syndrome with sensorineural deafness due to connexin 26 mutations.
Ibáñez MM; Alcalde MM; Jiménez MR; Muñoz MD; Díez-Delgado FJ
Pediatr Dermatol; 2013; 30(6):e138-42. PubMed ID: 23442195
[TBL] [Abstract][Full Text] [Related]
19. A novel p.Leu213X mutation in GJB2 gene in a Portuguese family.
Gonçalves AC; Chora J; Matos TD; Santos R; O'Neill A; Escada P; Fialho G; Caria H
Int J Pediatr Otorhinolaryngol; 2013 Jan; 77(1):89-91. PubMed ID: 23141775
[TBL] [Abstract][Full Text] [Related]
20. Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival.
Common JE; Di WL; Davies D; Kelsell DP
J Med Genet; 2004 Jul; 41(7):573-5. PubMed ID: 15235031
[No Abstract] [Full Text] [Related]
[Next] [New Search]