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PUBMED FOR HANDHELDS

Journal Abstract Search

319 related items for PubMed ID: 28012540

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  • 3. Frequency of GJB2 mutations, GJB6-D13S1830 and GJB6-D13S1854 deletions among patients with non-syndromic hearing loss from the central region of Iran.
    Naddafnia H, Noormohammadi Z, Irani S, Salahshoorifar I.
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00780. PubMed ID: 31162818
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  • 6. Screening of GJB6 gene large deletions among Syrians with congenital hearing impairment.
    Zaidieh T, Habbal W, Monem F.
    Genet Test Mol Biomarkers; 2015 Jul; 19(7):405-7. PubMed ID: 25989237
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  • 8. 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 Jul; 76(4):428-32. PubMed ID: 20835527
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  • 9. The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas.
    Küçük Kurtulgan H, Altuntaş EE, Yıldırım ME, Özdemir Ö, Bağcı B, Sezgin İ.
    J Int Adv Otol; 2019 Dec; 15(3):373-378. PubMed ID: 31846914
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  • 10. Analysis of the presence of the GJB6 mutations in patients heterozygous for GJB2 mutation in Brazil.
    Esteves MC, de Lima Isaac M, Francisco AM, da Silva Junior WA, Ferreira CA, Dell'Aringa AH.
    Eur Arch Otorhinolaryngol; 2014 Apr; 271(4):695-9. PubMed ID: 23553242
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  • 11. 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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  • 12. 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
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  • 13. 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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  • 14. Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.
    Haghighat-Nia A, Keivani A, Nadeali Z, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M.
    Int J Pediatr Otorhinolaryngol; 2015 Nov; 79(11):1892-5. PubMed ID: 26409293
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  • 15. The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions.
    Talbi S, Bonnet C, Boudjenah F, Mansouri MT, Petit C, Ammar Khodja F.
    Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():157-160. PubMed ID: 31200317
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  • 16. 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 Sep; 11(4):347-52. PubMed ID: 18294049
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  • 17. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
    Trabelsi M, Bahri W, Habibi M, Zainine R, Maazoul F, Ghazi B, Chaabouni H, Mrad R.
    Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199
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  • 18. 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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  • 19. Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients.
    Dalamón V, Béhèran A, Diamante F, Pallares N, Diamante V, Elgoyhen AB.
    Hear Res; 2005 Sep; 207(1-2):43-9. PubMed ID: 15964725
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  • 20. The digenic hypothesis unraveled: the GJB6 del(GJB6-D13S1830) mutation causes allele-specific loss of GJB2 expression in cis.
    Rodriguez-Paris J, Schrijver I.
    Biochem Biophys Res Commun; 2009 Nov 13; 389(2):354-9. PubMed ID: 19723508
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