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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

204 related items for PubMed ID: 11313763

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  • 3. 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
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  • 6. 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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  • 7. 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
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  • 11. A novel compound heterozygous mutation (35delG, 363delC) in the Connexin 26 gene causes non-syndromic autosomal recessive hearing loss.
    Onsori H, Rahmati M, Fazli D.
    Acta Med Iran; 2014 Dec; 52(8):638-40. PubMed ID: 25149889
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  • 14. Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss.
    Erbe CB, Harris KC, Runge-Samuelson CL, Flanary VA, Wackym PA.
    Laryngoscope; 2004 Apr; 114(4):607-11. PubMed ID: 15064611
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  • 17. A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness.
    Leshinsky-Silver E, Berman Z, Vinkler C, Yannov-Sharav M, Lev D.
    Hear Res; 2005 Apr; 202(1-2):258-61. PubMed ID: 15811717
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  • 19. Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL).
    Mishra S, Pandey H, Srivastava P, Mandal K, Phadke SR.
    Indian J Pediatr; 2018 Dec; 85(12):1061-1066. PubMed ID: 29542069
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  • 20. Distribution and phenotype of GJB2 mutations in 102 Sicilian patients with congenital non syndromic sensorineural hearing loss.
    Salvago P, Martines E, La Mattina E, Mucia M, Sammarco P, Sireci F, Martines F.
    Int J Audiol; 2014 Aug; 53(8):558-63. PubMed ID: 24793888
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