Works matching IS 10184813 AND DT 2006 AND VI 14 AND IP 4


Results: 15
    1
    2
    3
    4
    5
    6
    7
    8

    It's ‘back to school’ for genetic screening.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 4, p. 384, doi. 10.1038/sj.ejhg.5201581
    By:
    • Gason, Alexandra A.;
    • Delatycki, Martin B.;
    • Metcalfe, Sylvia A.;
    • Aitken, MaryAnne
    Publication type:
    Article
    9

    The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 4, p. 469, doi. 10.1038/sj.ejhg.5201582
    By:
    • Chang, Yen-Pei Christy;
    • Kim, James Dae-Ok;
    • Schwander, Karen;
    • Rao, Dabeeru C.;
    • Miller, Mike B.;
    • Weder, Alan B.;
    • Cooper, Richard S.;
    • Schork, Nicholas J.;
    • Province, Michael A.;
    • Morrison, Alanna C.;
    • Kardia, Sharon L. R.;
    • Quertermous, Thomas;
    • Chakravarti, Aravinda
    Publication type:
    Article
    10
    11
    12

    3000 years of solitude: extreme differentiation in the island isolates of Dalmatia, Croatia.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 4, p. 478, doi. 10.1038/sj.ejhg.5201589
    By:
    • Vitart, Veronique;
    • Biloglav, Zrinka;
    • Hayward, Caroline;
    • Janicijevic, Branka;
    • Smolej-Narancic, Nina;
    • Barac, Lovorka;
    • Pericic, Marijana;
    • Klaric, Irena Martinovic;
    • Skaric-Juric, Tatjana;
    • Barbalic, Maja;
    • Polasek, Ozren;
    • Kolcic, Ivana;
    • Carothers, Andrew;
    • Rudan, Pavao;
    • Hastie, Nick;
    • Wright, Alan;
    • Campbell, Harry;
    • Rudan, Igor
    Publication type:
    Article
    13

    Role of interferon-γ gene polymorphisms in susceptibility to IgA nephropathy: a family-based association study.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 4, p. 488, doi. 10.1038/sj.ejhg.5201591
    By:
    • Schena, Francesco Paolo;
    • Cerullo, Giuseppina;
    • Torres, Diletta Domenica;
    • Scolari, Francesco;
    • Foramitti, Marina;
    • Amoroso, Antonio;
    • Pirulli, Doroti;
    • Floege, Jürgen;
    • Mertens, Peter Rene;
    • Zerres, Klaus;
    • Alexopoulos, Efstathios;
    • Kirmizis, Dimitrios;
    • Zelante, Leopoldo;
    • Bisceglia, Luigi
    Publication type:
    Article
    14
    15

    Exonic microdeletions in the X-linked PQBP1 gene in mentally retarded patients: a pathogenic mutation and in-frame deletions of uncertain effect.

    Published in:
    European Journal of Human Genetics, 2006, v. 14, n. 4, p. 418, doi. 10.1038/sj.ejhg.5201593
    By:
    • Cossée, Mireille;
    • Demeer, Bénédicte;
    • Blanchet, Patricia;
    • Echenne, Bernard;
    • Singh, Deepika;
    • Hagens, Olivier;
    • Antin, Manuela;
    • Finck, Sonja;
    • Vallee, Louis;
    • Dollfus, Hélène;
    • Hegde, Sridevi;
    • Springell, Kelly;
    • Thelma, B. K.;
    • Woods, Geoffrey;
    • Kalscheuer, Vera;
    • Mandel, Jean-Louis
    Publication type:
    Article