Search Results - Raclin, V.

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  1. 1
    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 by Bürglen, L, Amiel, J, Viollet, L, Lefebvre, S, Burlet, P, Clermont, O, Raclin, V, Landrieu, P, Verloes, A, Munnich, A, Melki, J

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  2. 2
    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy

    Trinucleotide repeat contraction: a pitfall in prenatal diagnosis of myotonic dystrophy by Amiel, Jeanne, Raclin, Valérie, Jouannic, Jean-Marie, Morichon, Nicole, Hoffman-Radvanyi, Hélène, Dommergues, Marc, Feingold, Josué, Munnich, Arnold, Bonnefont, Jean-Paul

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  3. 3
    Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature

    Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature by Faivre, L., Morichon-Delvallez, N., Viot, G., Narcy, F., Loison, S., Mandelbrot, L., Aubry, M. C., Raclin, V., Edery, P., Munnich, A., Vekemans, M.

    Published in Prenatal diagnosis
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  4. 4
    Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature

    Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature by Faivre, L., Morichon-Delvallez, N., Viot, G., Martinovic, J., Pinson, M. P., Aubry, J. P., Raclin, V., Edery, P., Dumez, Y., Munnich, A., Vekemans, M.

    Published in Prenatal diagnosis
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  5. 5
    A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti

    A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti by Steffann, Julie, Raclin, Valérie, Smahi, Asmae, Woffendin, Hayley, Munnich, Arnold, Kenwrick, Sue J., Grebille, Anne-Gaelle, Benachi, Alexandra, Dumez, Yves, Bonnefont, Jean-Paul, Hadj-Rabia, Smaïl

    Published in Prenatal diagnosis
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  6. 6
    De novo deletions in spinal muscular atrophy: implications for genetic counselling

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

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  7. 7
    Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes

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

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  8. 8
    Prenatal diagnosis of respiratory chain deficiency by direct mutation screening

    Prenatal diagnosis of respiratory chain deficiency by direct mutation screening by Amiel, Jeanne, Gigarel, Nadine, Benacki, Alexandra, Benit, Paule, Valnot, Isabelle, Parfait, Béatrice, Von Kleist-Retzow, Jurgen-Christoph, Raclin, Valérie, Hadj-Rabia, Smaïl, Dumez, Yves, Rustin, Pierre, Bonnefont, Jean-Paul, Munnich, Arnold, Rötig, Agnès

    Published in Prenatal diagnosis
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  9. 9
    Délétion du gène SMN dans l'association arthrogrypose-amyotrophie spinale infantile

    Délétion du gène SMN dans l'association arthrogrypose-amyotrophie spinale infantile by Bürglen, L, Amiel, J, Viollet, L, Lefebre, S, Burlet, L, Clermont, O, Raclin, V, Landrieu, P, Verloes, A, Munnich, A, Melki, J

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  10. 10
    De novo deletions in spinal muscular atrophy: implications for genetic counselling

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

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