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Pubmed for Handhelds

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Journal Abstract Search

431 related items for PubMed ID: 16076412

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  • 23. 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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  • 24. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1).
    Cohn ES, Kelley PM, Fowler TW, Gorga MP, Lefkowitz DM, Kuehn HJ, Schaefer GB, Gobar LS, Hahn FJ, Harris DJ, Kimberling WJ.
    Pediatrics; 1999 Mar; 103(3):546-50. PubMed ID: 10049954
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  • 28. Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment.
    Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.
    Biochem Biophys Res Commun; 2009 Jul 31; 385(3):445-8. PubMed ID: 19465004
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  • 29. 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 31; 38(2):1309-13. PubMed ID: 20563649
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  • 31. 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 31; 269(6):1589-92. PubMed ID: 22037723
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  • 32. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.
    Rabionet R, Zelante L, López-Bigas N, D'Agruma L, Melchionda S, Restagno G, Arbonés ML, Gasparini P, Estivill X.
    Hum Genet; 2000 Jan 31; 106(1):40-4. PubMed ID: 10982180
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  • 37. Searching for digenic inheritance in deaf Brazilian individuals using the multiplex ligation-dependent probe amplification technique.
    da Silva-Costa SM, Martins FT, Pereira T, Pomilio MC, Marques-de-Faria AP, Sartorato EL.
    Genet Test Mol Biomarkers; 2011 Dec 31; 15(12):849-53. PubMed ID: 21728791
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  • 39. Sensorineural hearing loss and the incidence of Cx26 mutations in Austria.
    Löffler J, Nekahm D, Hirst-Stadlmann A, Günther B, Menzel HJ, Utermann G, Janecke AR.
    Eur J Hum Genet; 2001 Mar 31; 9(3):226-30. PubMed ID: 11313763
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