Search Results - Raclin, Valérie

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  1. 1
    Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas

    Characterization of three new deletions in the β-globin gene cluster during a screening survey in two French urban areas by Pissard, Serge, Raclin, Valérie, Lacan, Philippe, Garcia, Caroline, Aguilar-Martinez, Patricia, Francina, Alain, Joly, Philippe

    Published in Clinica chimica acta
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  2. 2
    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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  3. 3
    NDP gene mutations in 14 French families with Norrie disease

    NDP gene mutations in 14 French families with Norrie disease by Royer, Ghislaine, Hanein, Sylvain, Raclin, Valérie, Gigarel, Nadine, Rozet, Jean-Michel, Munnich, Arnold, Steffann, Julie, Dufier, Jean-Louis, Kaplan, Josseline, Bonnefont, Jean-Paul

    Published in Human mutation
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  4. 4
    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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  5. 5
    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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  6. 6
    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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