Canlyniadau Chwilio - Raclin, V

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  1. 1
    De novo deletions in spinal muscular atrophy: implications for genetic counselling.

    De novo deletions in spinal muscular atrophy: implications for genetic counselling. gan Raclin, V, Veber, P S, Bürglen, L, Munnich, A, Melki, J

    Cyhoeddwyd 1997
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  2. 2
    Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.

    Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes. gan Melki, J, Abdelhak, S, Burlet, P, Raclin, V, Kaplan, J, Spiegel, R, Gilgenkrantz, S, Philip, N, Chauvet, M L, Dumez, Y

    Cyhoeddwyd 1992
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  3. 3
    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy gan Amiel, J., Raclin, V., Jouannic, J., Morichon, N., Hoffman-Radvanyi, H., Dommergues, M., Feingold, J., Munnich, A., Bonnefont, J.

    Cyhoeddwyd 2001
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  4. 4
    Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association.

    Survival motor neuron gene deletion in the arthrogryposis multiplex congenita-spinal muscular atrophy association. gan Bürglen, L, Amiel, J, Viollet, L, Lefebvre, S, Burlet, P, Clermont, O, Raclin, V, Landrieu, P, Verloes, A, Munnich, A, Melki, J

    Cyhoeddwyd 1996
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