Search Results - Melançon, SergeB

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  1. 1
    Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism

    Carrier status diagnosis in Duchenne muscular dystrophy with "conformational" DNA polymorphism by Zietkiewicz, Ewa, Simard, LouiseR, Melançon, SergeB, Vanasse, Michel, Labuda, Damian

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  2. 2
    Molecular analyses of a lesch-Nyhan syndrome mutation (hprt MONTREAL) by use of T-lymphocyte cultures

    Molecular analyses of a lesch-Nyhan syndrome mutation (hprt MONTREAL) by use of T-lymphocyte cultures by SKOPEK, T. R, RECIO, L, SIMPSON, D, DALLAIRE, L, MELANCON, S. B, OGIER, H, O'NEILL, J. P, FALTA, M. T, NICKLAS, J. A, ALBERTINI, R. J

    Published in Human genetics
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    Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec

    Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec by Simard, L R, Gingras, F, Delvoye, N, Vanasse, M, Melançon, S B, Labuda, D

    Published in Human genetics
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