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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

91 related items for PubMed ID: 11558763

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  • 4. Longitudinal and cross-sectional phenotype analysis in a new, large Dutch DFNA2/KCNQ4 family.
    De Leenheer EM, Huygen PL, Coucke PJ, Admiraal RJ, van Camp G, Cremers CW.
    Ann Otol Rhinol Laryngol; 2002 Mar; 111(3 Pt 1):267-74. PubMed ID: 11915881
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  • 7. Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH.
    Bom SJ, Kemperman MH, Huygen PL, Luijendijk MW, Cremers CW.
    Ann Otol Rhinol Laryngol; 2003 Mar; 112(3):280-6. PubMed ID: 12656423
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  • 8. Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
    Verhoeven K, Fagerheim T, Prasad S, Wayne S, De Clau F, Balemans W, Verstreken M, Schatteman I, Solem B, Van de Heyning P, Tranebjärg L, Smith RJ, Van Camp G.
    Hum Genet; 2000 Jul; 107(1):7-11. PubMed ID: 10982027
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  • 11. Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusis.
    Oonk AM, Leijendeckers JM, Lammers EM, Weegerink NJ, Oostrik J, Beynon AJ, Huygen PL, Kunst HP, Kremer H, Snik AF, Pennings RJ.
    Hear Res; 2013 May; 299():88-98. PubMed ID: 23340379
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  • 12. The phenotype of DFNA13/COL11A2: nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.
    Kunst H, Huybrechts C, Marres H, Huygen P, Van Camp G, Cremers C.
    Am J Otol; 2000 Mar; 21(2):181-7. PubMed ID: 10733181
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  • 14. Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.
    Makishima T, Kurima K, Brewer CC, Griffith AJ.
    Otol Neurotol; 2004 Sep; 25(5):714-9. PubMed ID: 15354000
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  • 16. Audiologic phenotype of osteogenesis imperfecta: use in clinical differentiation.
    Swinnen FK, Dhooge IJ, Coucke PJ, D'Eufemia P, Zardo F, Garretsen TJ, Cremers CW, De Leenheer EM.
    Otol Neurotol; 2012 Feb; 33(2):115-22. PubMed ID: 22143304
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  • 20. A novel EYA4 mutation causing hearing loss in a Chinese DFNA family and genotype-phenotype review of EYA4 in deafness.
    Huang A, Yuan Y, Liu Y, Zhu Q, Dai P.
    J Transl Med; 2015 May 12; 13():154. PubMed ID: 25963406
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