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Journal Abstract Search

99 related items for PubMed ID: 3162715

  • 21. Hearing loss in Usher syndrome type II is nonprogressive.
    Reisser CF, Kimberling WJ, Otterstedde CR.
    Ann Otol Rhinol Laryngol; 2002 Dec; 111(12 Pt 1):1108-11. PubMed ID: 12498372
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  • 22. USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian allele.
    Ouyang XM, Hejtmancik JF, Jacobson SG, Xia XJ, Li A, Du LL, Newton V, Kaiser M, Balkany T, Nance WE, Liu XZ.
    Clin Genet; 2003 Feb; 63(2):150-3. PubMed ID: 12630964
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  • 24. Clinical findings in obligate carriers of type I Usher syndrome.
    Wagenaar M, ter Rahe B, van Aarem A, Huygen P, Admiraal R, Bleeker-Wagemakers E, Pinckers A, Kimberling W, Cremers C.
    Am J Med Genet; 1995 Nov 20; 59(3):375-9. PubMed ID: 8599365
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  • 27. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
    Hmani M, Ghorbel A, Boulila-Elgaied A, Ben Zina Z, Kammoun W, Drira M, Chaabouni M, Petit C, Ayadi H.
    Eur J Hum Genet; 1999 Apr 20; 7(3):363-7. PubMed ID: 10234513
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  • 29. Evidence for a fourth locus in Usher syndrome type I.
    Gerber S, Larget-Piet D, Rozet JM, Bonneau D, Mathieu M, Der Kaloustian V, Munnich A, Kaplan J.
    J Med Genet; 1996 Jan 20; 33(1):77-9. PubMed ID: 8825055
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  • 30. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
    Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D.
    Hum Genet; 2002 Apr 20; 110(4):348-50. PubMed ID: 11941484
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  • 31. Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome.
    Keogh IJ, Godinho RN, Wu TP, Diaz de Palacios AM, Palacios N, Bello de Alford M, De Almada MI, MarPalacios N, Vazquez A, Mattei R, Seidman C, Seidman J, Eavey RD.
    Int J Pediatr Otorhinolaryngol; 2004 Aug 20; 68(8):1063-8. PubMed ID: 15236894
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  • 35. Spectrum of mutations in USH2A in British patients with Usher syndrome type II.
    Leroy BP, Aragon-Martin JA, Weston MD, Bessant DA, Willis C, Webster AR, Bird AC, Kimberling WJ, Payne AM, Bhattacharya SS.
    Exp Eye Res; 2001 May 20; 72(5):503-9. PubMed ID: 11311042
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  • 36. Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
    Eudy JD, Weston MD, Yao S, Hoover DM, Rehm HL, Ma-Edmonds M, Yan D, Ahmad I, Cheng JJ, Ayuso C, Cremers C, Davenport S, Moller C, Talmadge CB, Beisel KW, Tamayo M, Morton CC, Swaroop A, Kimberling WJ, Sumegi J.
    Science; 1998 Jun 12; 280(5370):1753-7. PubMed ID: 9624053
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