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Journal Abstract Search

286 related items for PubMed ID: 17368814

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  • 2. 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
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  • 4. 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
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  • 6. 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
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  • 7. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.
    Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Reiisi S, Pourreza MR, Noori-Daloii MR, Tabatabaiefar MA.
    Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():121-126. PubMed ID: 29501291
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  • 12. 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
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  • 13. Frequency of GJB2 and del(GJB6-D13S1830) mutations among an Ecuadorian mestizo population.
    Paz-y-Miño C, Beaty D, López-Cortés A, Proaño I.
    Int J Pediatr Otorhinolaryngol; 2014 Oct; 78(10):1648-54. PubMed ID: 25085072
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  • 14. Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness.
    Belintani Piatto V, Maria Goloni Bertollo E, Lúcia Sartorato E, Victor Maniglia J.
    Hear Res; 2004 Oct; 196(1-2):87-93. PubMed ID: 15464305
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  • 17. 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
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  • 20. Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria.
    Frei K, Ramsebner R, Lucas T, Baumgartner WD, Schoefer C, Wachtler FJ, Kirschhofer K.
    Hear Res; 2004 Oct; 196(1-2):115-8. PubMed ID: 15464308
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