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Journal Abstract Search

99 related items for PubMed ID: 3162715

  • 41. Localization of two genes for Usher syndrome type I to chromosome 11.
    Smith RJ, Lee EC, Kimberling WJ, Daiger SP, Pelias MZ, Keats BJ, Jay M, Bird A, Reardon W, Guest M.
    Genomics; 1992 Dec; 14(4):995-1002. PubMed ID: 1478678
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  • 42. 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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  • 43. Presumed drusen of optic nerve head in siblings with Usher syndrome.
    Shiono T, Noro M, Tamai M.
    Jpn J Ophthalmol; 1991 Aug 19; 35(3):300-5. PubMed ID: 1770670
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  • 44. Two families from New England with usher syndrome type IC with distinct haplotypes.
    DeAngelis MM, McGee TL, Keats BJ, Slim R, Berson EL, Dryja TP.
    Am J Ophthalmol; 2001 Mar 19; 131(3):355-8. PubMed ID: 11239869
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  • 48. Usher syndrome type III can mimic other types of Usher syndrome.
    Pennings RJ, Fields RR, Huygen PL, Deutman AF, Kimberling WJ, Cremers CW.
    Ann Otol Rhinol Laryngol; 2003 Jun 19; 112(6):525-30. PubMed ID: 12834121
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  • 56. Usher syndrome: clinical findings and gene localization studies.
    Kimberling WJ, Möller CG, Davenport SL, Lund G, Grissom TJ, Priluck I, White V, Weston MD, Biscone-Halterman K, Brookhouser PE.
    Laryngoscope; 1989 Jan 19; 99(1):66-72. PubMed ID: 2562904
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  • 60. Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.
    Nájera C, Beneyto M, Blanca J, Aller E, Fontcuberta A, Millán JM, Ayuso C.
    Hum Mutat; 2002 Jul 19; 20(1):76-7. PubMed ID: 12112664
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