Works matching AU Grancho, Maria


Results: 2
    1
    2

    The 1396del a mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer.

    Published in:
    Human Mutation, 1998, v. 11, n. 5, p. 413, doi. 10.1002/(SICI)1098-1004(1998)11:5<413::AID-HUMU18>3.0.CO;2-C
    By:
    • Vidal, Véronique;
    • Bay, Jacques-Olivier;
    • Champomier, Françoise;
    • Grancho, Maria;
    • Beauville, Laurence;
    • Glowaczower, Cécile;
    • Lemery, Didier;
    • Ferrara, Marc;
    • Bignon, Yves-Jean
    Publication type:
    Article