Hasil Pencarian - Gille Johan JP

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  1. 1
    The frequent <it>BRCA1 </it>mutation 1135insA has multiple origins: a haplotype study in different populations

    The frequent <it>BRCA1 </it>mutation 1135insA has multiple origins: a haplotype study in different populations oleh Møller Pål, Gille Johan JP, Hogervorst Frans, Galvez Maria, Hamel Nancy, Rudkin Teresa M, Apold Jaran, Foulkes William D

    Diterbitkan 2006-03-01
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  2. 2
    A novel pathogenic <it>MLH1 </it>missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome

    A novel pathogenic <it>MLH1 </it>missense mutation, c.112A > C, p.Asn38His, in six families with Lynch syndrome oleh van Riel Els, Ausems Margreet GEM, Hogervorst Frans BL, Kluijt Irma, van Gijn Marielle E, van Echtelt Jeanne, Scheidel-Jacobse Karen, Hennekam Eric FAM, Stulp Rein P, Vos Yvonne J, Offerhaus G Johan A, Menko Fred H, Gille Johan JP

    Diterbitkan 2010-08-01
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