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Journal Abstract Search

87 related items for PubMed ID: 9411747

  • 1.
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  • 2. Two deaf mice, two deaf mice..
    Heller S, Hudspeth AJ.
    Nat Med; 1998 May; 4(5):560-1. PubMed ID: 9585227
    [No Abstract] [Full Text] [Related]

  • 3.
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  • 4. Hair hear!
    Phimister B.
    Nat Genet; 1998 May; 19(1):8. PubMed ID: 9590277
    [No Abstract] [Full Text] [Related]

  • 5.
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  • 6. Deafness. Sounds from the cochlea.
    Avraham KB.
    Nature; 1997 Dec 11; 390(6660):559-60. PubMed ID: 9403680
    [No Abstract] [Full Text] [Related]

  • 7. More deafness genes.
    Steel KP, Brown SD.
    Science; 1998 May 29; 280(5368):1403. PubMed ID: 9634418
    [No Abstract] [Full Text] [Related]

  • 8. Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous.
    Lynch ED, Lee MK, Morrow JE, Welcsh PL, León PE, King MC.
    Science; 1997 Nov 14; 278(5341):1315-8. PubMed ID: 9360932
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  • 10. DFNB3 families and Shaker-2 mice: mutations in an unconventional myosin, myo 15.
    Friedman TB, Hinnant JT, Fridell RA, Wilcox ER, Raphael Y, Camper SA.
    Adv Otorhinolaryngol; 2000 Nov 14; 56():131-44. PubMed ID: 10868225
    [No Abstract] [Full Text] [Related]

  • 11. Inner Ear Connexin Channels: Roles in Development and Maintenance of Cochlear Function.
    Mammano F.
    Cold Spring Harb Perspect Med; 2019 Jul 01; 9(7):. PubMed ID: 30181354
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  • 13. The genetic bases for syndromic and nonsyndromic deafness among Jews.
    Ben-Yosef T, Friedman TB.
    Trends Mol Med; 2003 Nov 01; 9(11):496-502. PubMed ID: 14604828
    [Abstract] [Full Text] [Related]

  • 14. Deaf and dizzy mice with mutated myosin motors.
    Gillespie PG.
    Nat Med; 1996 Jan 01; 2(1):27-9. PubMed ID: 8564830
    [No Abstract] [Full Text] [Related]

  • 15. [New molecular genetic knowledge on development of hereditary deafness].
    Pfister M.
    HNO; 1998 Sep 01; 46(9):782-4. PubMed ID: 9816530
    [No Abstract] [Full Text] [Related]

  • 16. Mechanism of the defect in gap-junctional communication by expression of a connexin 26 mutant associated with dominant deafness.
    Chen Y, Deng Y, Bao X, Reuss L, Altenberg GA.
    FASEB J; 2005 Sep 01; 19(11):1516-8. PubMed ID: 16009703
    [Abstract] [Full Text] [Related]

  • 17. Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.
    Ahmed ZM, Smith TN, Riazuddin S, Makishima T, Ghosh M, Bokhari S, Menon PS, Deshmukh D, Griffith AJ, Riazuddin S, Friedman TB, Wilcox ER.
    Hum Genet; 2002 Jun 01; 110(6):527-31. PubMed ID: 12107438
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