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Journal Abstract Search

137 related items for PubMed ID: 2241083

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  • 8. 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; 7(3):363-7. PubMed ID: 10234513
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  • 11. Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.
    Bruford EA, Riise R, Teague PW, Porter K, Thomson KL, Moore AT, Jay M, Warburg M, Schinzel A, Tommerup N, Tornqvist K, Rosenberg T, Patton M, Mansfield DC, Wright AF.
    Genomics; 1997 Apr 01; 41(1):93-9. PubMed ID: 9126487
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  • 13. [Clinical examinations in Usher's syndrome].
    Lubiński W, Palacz O, Zajaczek S.
    Klin Oczna; 1996 Jan 01; 98(1):55-8. PubMed ID: 9019578
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  • 17. In our parents' shadow, Usher's syndrome.
    Gelbart M.
    Nurs Times; 1996 Jan 01; 94(34):35. PubMed ID: 9791511
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  • 19. An unusual otological manifestation of Usher's syndrome in four siblings.
    Karjalainen S, Teräsvirta M, Kärjä J, Kääriäinen H.
    Clin Genet; 1983 Oct 01; 24(4):273-9. PubMed ID: 6641004
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