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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]
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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. 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]
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. [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. 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. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2. Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641 [TBL] [Abstract][Full Text] [Related]
10. 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]
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12. 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]
13. [Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary]. Tóth T; Kupka S; Blin N; Pfister M; Sziklai I Orv Hetil; 2002 Oct; 143(40):2285-9. PubMed ID: 12420583 [TBL] [Abstract][Full Text] [Related]
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16. 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]
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18. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. del Castillo I; Villamar M; Moreno-Pelayo MA; del Castillo FJ; Alvarez A; Tellería D; Menéndez I; Moreno F N Engl J Med; 2002 Jan; 346(4):243-9. PubMed ID: 11807148 [TBL] [Abstract][Full Text] [Related]
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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]