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Journal Abstract Search

100 related items for PubMed ID: 10704186

  • 1. Autosomal recessive nonsyndromic hearing loss.
    Sundstrom RA, Van Laer L, Van Camp G, Smith RJ.
    Am J Med Genet; 1999 Sep 24; 89(3):123-9. PubMed ID: 10704186
    [Abstract] [Full Text] [Related]

  • 2. Autosomal dominant nonsyndromic hearing impairment.
    Van Laer L, McGuirt WT, Yang T, Smith RJ, Van Camp G.
    Am J Med Genet; 1999 Sep 24; 89(3):167-74. PubMed ID: 10704191
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive nonsyndromic deafness genes: a review.
    Duman D, Tekin M.
    Front Biosci (Landmark Ed); 2012 Jun 01; 17(6):2213-36. PubMed ID: 22652773
    [Abstract] [Full Text] [Related]

  • 4. Identification of autosomal recessive nonsyndromic hearing impairment genes through the study of consanguineous and non-consanguineous families: past, present, and future.
    Acharya A, Schrauwen I, Leal SM.
    Hum Genet; 2022 Apr 01; 141(3-4):413-430. PubMed ID: 34291353
    [Abstract] [Full Text] [Related]

  • 5. A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.
    Ansar M, Din MA, Arshad M, Sohail M, Faiyaz-Ul-Haque M, Haque S, Ahmad W, Leal SM.
    Eur J Hum Genet; 2003 Jan 01; 11(1):77-80. PubMed ID: 12529709
    [Abstract] [Full Text] [Related]

  • 6. Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss.
    Xia H, Huang X, Guo Y, Hu P, He G, Deng X, Xu H, Yang Z, Deng H.
    PLoS One; 2015 Jan 01; 10(8):e0136306. PubMed ID: 26308726
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  • 9. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
    Liu XZ, Walsh J, Mburu P, Kendrick-Jones J, Cope MJ, Steel KP, Brown SD.
    Nat Genet; 1997 Jun 01; 16(2):188-90. PubMed ID: 9171832
    [Abstract] [Full Text] [Related]

  • 10. Non-syndromic autosomal-dominant deafness.
    Petersen MB.
    Clin Genet; 2002 Jul 01; 62(1):1-13. PubMed ID: 12123480
    [Abstract] [Full Text] [Related]

  • 11. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
    Ansar M, Ramzan M, Pham TL, Yan K, Jamal SM, Haque S, Ahmad W, Leal SM.
    Hum Hered; 2003 Jul 01; 55(1):71-4. PubMed ID: 12890929
    [Abstract] [Full Text] [Related]

  • 12. Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss.
    Zhang J, Guan J, Wang H, Yin L, Wang D, Zhao L, Zhou H, Wang Q.
    BMC Med Genet; 2019 Apr 05; 20(1):60. PubMed ID: 30953472
    [Abstract] [Full Text] [Related]

  • 13. Deafness genes.
    Kitamura K, Takahashi K, Tamagawa Y, Noguchi Y, Kuroishikawa Y, Ishikawa K, Hagiwara H.
    J Med Dent Sci; 2000 Mar 05; 47(1):1-11. PubMed ID: 12162522
    [Abstract] [Full Text] [Related]

  • 14. Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53.
    Chakchouk I, Grati M, Bademci G, Bensaid M, Ma Q, Chakroun A, Foster J, Yan D, Duman D, Diaz-Horta O, Ghorbel A, Mittal R, Farooq A, Tekin M, Masmoudi S, Liu XZ.
    Mol Genet Genomics; 2015 Aug 05; 290(4):1327-34. PubMed ID: 25633957
    [Abstract] [Full Text] [Related]

  • 15. Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.
    Liburd N, Ghosh M, Riazuddin S, Naz S, Khan S, Ahmed Z, Riazuddin S, Liang Y, Menon PS, Smith T, Smith AC, Chen KS, Lupski JR, Wilcox ER, Potocki L, Friedman TB.
    Hum Genet; 2001 Nov 05; 109(5):535-41. PubMed ID: 11735029
    [Abstract] [Full Text] [Related]

  • 16. Connexin 26 mutations in nonsyndromic autosomal recessive hearing loss: speech and hearing rehabilitation.
    Mesolella M, Tranchino G, Nardone M, Motta S, Galli V.
    Int J Pediatr Otorhinolaryngol; 2004 Aug 05; 68(8):995-1005. PubMed ID: 15236885
    [Abstract] [Full Text] [Related]

  • 17. Genetics of hearing and deafness.
    Angeli S, Lin X, Liu XZ.
    Anat Rec (Hoboken); 2012 Nov 05; 295(11):1812-29. PubMed ID: 23044516
    [Abstract] [Full Text] [Related]

  • 18. Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness.
    Lezirovitz K, Pardono E, de Mello Auricchio MT, de Carvalho E Silva FL, Lopes JJ, Abreu-Silva RS, Romanos J, Batissoco AC, Mingroni-Netto RC.
    Eur J Hum Genet; 2008 Jan 05; 16(1):89-96. PubMed ID: 17851452
    [Abstract] [Full Text] [Related]

  • 19. At the speed of sound: gene discovery in the auditory system.
    Resendes BL, Williamson RE, Morton CC.
    Am J Hum Genet; 2001 Nov 05; 69(5):923-35. PubMed ID: 11577373
    [Abstract] [Full Text] [Related]

  • 20. Autosomal recessive nonsyndromal profound childhood deafness in a large pedigree. Audiometric features of the affected persons and the obligate carriers.
    Marres HA, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 1989 May 05; 115(5):591-5. PubMed ID: 2706105
    [Abstract] [Full Text] [Related]

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