These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
260 related articles for article (PubMed ID: 22037723)
1. 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]
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. Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania. Lazăr C; Popp R; Trifa A; Mocanu C; Mihut G; Al-Khzouz C; Tomescu E; Figan I; Grigorescu-Sido P Int J Pediatr Otorhinolaryngol; 2010 Apr; 74(4):351-5. PubMed ID: 20096468 [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. 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]
6. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates. Hochman JB; Stockley TL; Shipp D; Lin VY; Chen JM; Nedzelski JM Otol Neurotol; 2010 Aug; 31(6):919-22. PubMed ID: 20601923 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Prevalence of mutations located at the dfnb1 locus in a population of cochlear implanted children in eastern Romania. Rădulescu L; Mârţu C; Birkenhäger R; Cozma S; Ungureanu L; Laszig R Int J Pediatr Otorhinolaryngol; 2012 Jan; 76(1):90-4. PubMed ID: 22070872 [TBL] [Abstract][Full Text] [Related]
16. Frequency of GJB2 mutations in patients with nonsyndromic hearing loss from an ethnically characterized Brazilian population. Felix F; Ribeiro MG; Tomita S; Zalis MG Braz J Otorhinolaryngol; 2019; 85(1):92-98. PubMed ID: 29773520 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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] [Next] [New Search]