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PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 11889386

  • 1. Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation.
    Tamagawa Y, Ishikawa K, Ishikawa K, Ishida T, Kitamura K, Makino S, Tsuru T, Ichimura K.
    Laryngoscope; 2002 Feb; 112(2):292-7. PubMed ID: 11889386
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  • 8. In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.
    Kallman JC, Phillips JO, Bramhall NF, Kelly JP, Street VA.
    Otol Neurotol; 2008 Sep; 29(6):860-7. PubMed ID: 18667942
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  • 9. Further characterization of the DFNA1 audiovestibular phenotype.
    Lalwani AK, Jackler RK, Sweetow RW, Lynch ED, Raventós H, Morrow J, King MC, León PE.
    Arch Otolaryngol Head Neck Surg; 1998 Jun; 124(6):699-702. PubMed ID: 9639482
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  • 11. Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.
    Weegerink NJ, Huygen PL, Schraders M, Kremer H, Pennings RJ, Kunst HP.
    Hear Res; 2011 Dec; 282(1-2):167-77. PubMed ID: 21893181
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  • 13. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
    Kumar A, Babu M, Kimberling WJ, Venkatesh CP.
    Mol Vis; 2004 Nov 24; 10():910-6. PubMed ID: 15592175
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  • 14. Searching for evidence of DFNB2.
    Astuto LM, Kelley PM, Askew JW, Weston MD, Smith RJ, Alswaid AF, Al-Rakaf M, Kimberling WJ.
    Am J Med Genet; 2002 May 15; 109(4):291-7. PubMed ID: 11992483
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  • 15. Identification of three novel mutations in the MYO7A gene.
    Cuevas JM, Espinós C, Millán JM, Sánchez F, Trujillo MJ, Ayuso C, Beneyto M, Nájera C.
    Hum Mutat; 1999 Aug 19; 14(2):181. PubMed ID: 10447383
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  • 16. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
    Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ.
    J Assoc Res Otolaryngol; 2007 Mar 19; 8(1):1-7. PubMed ID: 17136632
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  • 17. Clinical Profiles of DFNA11 at Diverse Stages of Development and Aging in a Large Family Identified by Linkage Analysis.
    Yamamoto N, Mutai H, Namba K, Goto F, Ogawa K, Matsunaga T.
    Otol Neurotol; 2020 Jul 19; 41(6):e663-e673. PubMed ID: 32097363
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  • 19. Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).
    Luijendijk MW, Van Wijk E, Bischoff AM, Krieger E, Huygen PL, Pennings RJ, Brunner HG, Cremers CW, Cremers FP, Kremer H.
    Hum Genet; 2004 Jul 19; 115(2):149-56. PubMed ID: 15221449
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  • 20. Progressive sensorineural hearing loss in children with mitochondrial encephalomyopathies.
    Zwirner P, Wilichowski E.
    Laryngoscope; 2001 Mar 19; 111(3):515-21. PubMed ID: 11224785
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