160 related articles for article (PubMed ID: 20059378)
1. Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.
Kokotas H; Grigoriadou M; Hatzaki A; Antoniadi T; Giannoulia-Karantana A; Petersen MB
Genet Test Mol Biomarkers; 2010 Apr; 14(2):189-92. PubMed ID: 20059378
[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. 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]
4. High frequency of 35delG GJB2 mutation and absence of del(GJB6-D13S1830) in Greek Cypriot patients with nonsyndromic hearing loss.
Neocleous V; Aspris A; Shahpenterian V; Nicolaou V; Panagi C; Ioannou I; Kyamides Y; Anastasiadou V; Phylactou LA
Genet Test; 2006; 10(4):285-9. PubMed ID: 17253936
[TBL] [Abstract][Full Text] [Related]
5. Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method.
Storm K; Willocx S; Flothmann K; Van Camp G
Hum Mutat; 1999; 14(3):263-6. PubMed ID: 10477435
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
Tlili A; Al Mutery A; Kamal Eddine Ahmad Mohamed W; Mahfood M; Hadj Kacem H
Genet Test Mol Biomarkers; 2017 Nov; 21(11):686-691. PubMed ID: 29016196
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. 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]
9. 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]
10. 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]
11. Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
Abidi O; Boulouiz R; Nahili H; Bakhouch K; Wakrim L; Rouba H; Chafik A; Hassar M; Barakat A
Genet Test; 2008 Dec; 12(4):569-74. PubMed ID: 19072567
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness.
Antoniadi T; Grønskov K; Sand A; Pampanos A; Brøndum-Nielsen K; Petersen MB
Hum Mutat; 2000; 16(1):7-12. PubMed ID: 10874298
[TBL] [Abstract][Full Text] [Related]
14. Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss.
Utrera R; Ridaura V; Rodríguez Y; Rojas MJ; Mago L; Angeli S; Henríquez O
Genet Test; 2007; 11(4):347-52. PubMed ID: 18294049
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness.
Pallares-Ruiz N; Blanchet P; Mondain M; Low-Hong S; Demaille J; Claustres M; Roux AF
Genet Test; 2001; 5(4):339-43. PubMed ID: 11960582
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population.
Kokotas H; Van Laer L; Grigoriadou M; Iliadou V; Economides J; Pomoni S; Pampanos A; Eleftheriades N; Ferekidou E; Korres S; Giannoulia-Karantana A; Van Camp G; Petersen MB
Am J Med Genet A; 2008 Nov; 146A(22):2879-84. PubMed ID: 18925674
[TBL] [Abstract][Full Text] [Related]
19. GJB2 mutations in the Swiss hearing impaired.
Gürtler N; Kim Y; Mhatre A; Müller R; Probst R; Lalwani AK
Ear Hear; 2003 Oct; 24(5):440-7. PubMed ID: 14534413
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
