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Journal Abstract Search

400 related items for PubMed ID: 18554165

  • 1. 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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  • 6. 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
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  • 10. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Al-Achkar W, Al-Halabi B, Ali B, Moassass F.
    Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():82-87. PubMed ID: 28012540
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  • 11. Connexin 26 and 30 mutations in paediatric patients with congenital, non-syndromic hearing loss treated with cochlear implantation in Mediterranean Turkey.
    Tarkan Ö, Sari P, Demirhan O, Kiroğlu M, Tuncer Ü, Sürmelioğlu Ö, Ozdemir S, Yilmaz MB, Kara K.
    J Laryngol Otol; 2013 Jan; 127(1):33-7. PubMed ID: 23171692
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  • 15. 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 30; 121A(2):102-8. PubMed ID: 12910486
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  • 16. 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 30; 76(2):268-71. PubMed ID: 22172221
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  • 20. Double heterozygosity with mutations involving both the GJB2 and GJB6 genes is a possible, but very rare, cause of congenital deafness in the Czech population.
    Seeman P, Bendová O, Rasková D, Malíková M, Groh D, Kabelka Z.
    Ann Hum Genet; 2005 Jan 30; 69(Pt 1):9-14. PubMed ID: 15638823
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