77 related articles for article (PubMed ID: 26681637)
1. Two molecular assays for the rapid and inexpensive detection of GJB2 and GJB6 mutations.
Cascella R; Strafella C; Gambardella S; Longo G; Borgiani P; Sangiuolo F; Novelli G; Giardina E
Electrophoresis; 2016 Mar; 37(5-6):860-4. PubMed ID: 26681637
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Absence of GJB6 mutations in Indian patients with non-syndromic hearing loss.
Bhalla S; Sharma R; Khandelwal G; Panda NK; Khullar M
Int J Pediatr Otorhinolaryngol; 2011 Mar; 75(3):356-9. PubMed ID: 21227513
[TBL] [Abstract][Full Text] [Related]
4. Mutations in GJB2, GJB6, and mitochondrial DNA are rare in African American and Caribbean Hispanic individuals with hearing impairment.
Samanich J; Lowes C; Burk R; Shanske S; Lu J; Shanske A; Morrow BE
Am J Med Genet A; 2007 Apr; 143A(8):830-8. PubMed ID: 17357124
[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. Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele.
Gualandi E; Ravani A; Berto A; Burdo S; Trevisi P; Ferlini A; Martini A; Calzolari E
Acta Otolaryngol Suppl; 2004 May; (552):29-34. PubMed ID: 15219044
[TBL] [Abstract][Full Text] [Related]
7. The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
Bazazzadegan N; Nikzat N; Fattahi Z; Nishimura C; Meyer N; Sahraian S; Jamali P; Babanejad M; Kashef A; Yazdan H; Sabbagh Kermani F; Taghdiri M; Azadeh B; Mojahedi F; Khoshaeen A; Habibi H; Reyhanifar F; Nouri N; Smith RJ; Kahrizi K; Najmabadi H
Int J Pediatr Otorhinolaryngol; 2012 Aug; 76(8):1164-74. PubMed ID: 22695344
[TBL] [Abstract][Full Text] [Related]
8. Spectrum of GJB2 mutations in a cohort of nonsyndromic hearing loss cases from the Kingdom of Saudi Arabia.
Al-Qahtani MH; Baghlab I; Chaudhary AG; Abuzenadah AM; Bamanie A; Daghistani KJ; Safieh M; Fida L; Dallol A
Genet Test Mol Biomarkers; 2010 Feb; 14(1):79-83. PubMed ID: 19929407
[TBL] [Abstract][Full Text] [Related]
9. Use of a multiplex PCR/sequencing strategy to detect both connexin 30 (GJB6) 342 kb deletion and connexin 26 (GJB2) mutations in cases of childhood deafness.
Wu BL; Kenna M; Lip V; Irons M; Platt O
Am J Med Genet A; 2003 Aug; 121A(2):102-8. PubMed ID: 12910486
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects.
Fitzgerald T; Duva S; Ostrer H; Pass K; Oddoux C; Ruben R; Caggana M
Clin Genet; 2004 Apr; 65(4):338-42. PubMed ID: 15025729
[TBL] [Abstract][Full Text] [Related]
12. A novel connexin 26 compound heterozygous mutation results in deafness.
Harris KC; Erbe CB; Firszt JB; Flanary VA; Wackym PA
Laryngoscope; 2002 Jul; 112(7 Pt 1):1159-62. PubMed ID: 12169891
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Prevalence of Deafness-Associated Connexin-26 (GJB2) and Connexin-30 (GJB6) Pathogenic Alleles in a Large Patient Cohort from Eastern Sicily.
Amorini M; Romeo P; Bruno R; Galletti F; Di Bella C; Longo P; Briuglia S; Salpietro C; Rigoli L
Ann Hum Genet; 2015 Sep; 79(5):341-349. PubMed ID: 26096904
[TBL] [Abstract][Full Text] [Related]
15. A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?
Pallares-Ruiz N; Blanchet P; Mondain M; Claustres M; Roux AF
Eur J Hum Genet; 2002 Jan; 10(1):72-6. PubMed ID: 11896458
[TBL] [Abstract][Full Text] [Related]
16. Mutation analysis of the Cx26, Cx30, and Cx31 genes in autosomal recessive nonsyndromic hearing impairment.
Gürtler N; Egenter C; Bösch N; Plasilova M
Acta Otolaryngol; 2008 Oct; 128(10):1056-62. PubMed ID: 18607988
[TBL] [Abstract][Full Text] [Related]
17. Multiplex detection of common mutations in the Connexin-26 gene.
Baris I; Köksal V
Genet Test; 2003; 7(1):63-5. PubMed ID: 12820705
[TBL] [Abstract][Full Text] [Related]
18. [Hereditary deafness in Kirov oblast: estimation of the incidence rate and DNA diagnosis in children].
Zinchenko RA; Osetrova AA; Sharonova EI
Genetika; 2012 Apr; 48(4):542-50. PubMed ID: 22730774
[TBL] [Abstract][Full Text] [Related]
19. Spectrum of Genes for Non-
Shatokhina O; Galeeva N; Stepanova A; Markova T; Lalayants M; Alekseeva N; Tavarkiladze G; Markova T; Bessonova L; Petukhova M; Guseva D; Anisimova I; Polyakov A; Ryzhkova O; Bliznetz E
Int J Mol Sci; 2022 Dec; 23(24):. PubMed ID: 36555390
[TBL] [Abstract][Full Text] [Related]
20. The Functional Role of CONNEXIN 26 Mutation in Nonsyndromic Hearing Loss, Demonstrated by Zebrafish Connexin 30.3 Homologue Model.
Su HA; Lai TW; Li SY; Su TR; Yang JJ; Su CC
Cells; 2020 May; 9(5):. PubMed ID: 32455934
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
