Works matching IS 03406717 AND DT 2004 AND VI 114 AND IP 6

Results: 14
    1

    Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis.

    Published in:
    Human Genetics, 2004, v. 114, n. 6, p. 573, doi. 10.1007/s00439-004-1095-9
    By:
    • Rubio, Justin P.;
    • Bahlo, Melanie;
    • Tubridy, Niall;
    • Stankovich, Jim;
    • Burfoot, Rachel;
    • Butzkueven, Helmut;
    • Chapman, Caron;
    • Johnson, Laura;
    • Marriott, Mark;
    • Mraz, Grant;
    • Tait, Brian;
    • Wilkinson, Chris;
    • Taylor, Bruce;
    • Speed, Terence P.;
    • Foote, Simon J.;
    • Kilpatrick, Trevor J.
    Publication type:
    Article
    2
    3

    Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.

    Published in:
    Human Genetics, 2004, v. 114, n. 6, p. 534, doi. 10.1007/s00439-004-1100-3
    By:
    • Langan, Joanne E.;
    • Cole, Charlotte G.;
    • Huckle, Elisabeth J.;
    • Byrne, Shaun;
    • McRonald, Fiona E.;
    • Rowbottom, Lynn;
    • Ellis, Anthony;
    • Shaw, Joan M.;
    • Leigh, Irene M.;
    • Kelsell, David P.;
    • Dunham, Ian;
    • Field, John K.;
    • Risk, Janet M.
    Publication type:
    Article
    4
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    9

    Fine mapping of the Schnyder’s crystalline corneal dystrophy locus.

    Published in:
    Human Genetics, 2004, v. 114, n. 6, p. 594, doi. 10.1007/s00439-004-1110-1
    By:
    • Theendakara, Veena;
    • Tromp, Gerard;
    • Kuivaniemi, Helena;
    • White, Peter S.;
    • Panchal, Seema;
    • Cox, Jennifer;
    • Winters, R. Scott;
    • Riebeling, Petra;
    • Tost, Frank;
    • Hoeltzenbein, Maria;
    • Tervo, Timo M.;
    • Henn, Wolfram;
    • Denniger, Elke;
    • Krause, Matthias;
    • Koksal, Murat;
    • Kargi, Sebnem;
    • Ugurbas, Suat H.;
    • Latvala, Terho;
    • Shearman, Amanda M.;
    • Weiss, Jayne S.
    Publication type:
    Article
    10
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    Mutations.

    Published in:
    2004
    Publication type:
    Table of Contents
    14