检索结果 - Myrtille Spentchian

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  1. 1
    International Registry of Patients Carrying <i>TGFBR1</i> or <i>TGFBR2</i> Mutations

    International Registry of Patients Carrying <i>TGFBR1</i> or <i>TGFBR2</i> Mutations 由 Guillaume Jondeau, Jacques Ropers, Ellen S. Regalado, Alan C. Braverman, Arturo Evangelista, G Teixedo, Julie De Backer, Laura Muiño Mosquera, Sophie Naudion, Cécile Zordan, Takayuki Morisaki, Hiroto Morisaki, Yskert Von Kodolitsch, Sophie Dupuis‐Girod, Shaine A. Morris, Richmond Jeremy, Sylvie Odent, Leslie C. Adès, Madhura Bakshi, Katherine Holman, Scott A. LeMaire, Olivier Milleron, Maud Langeois, Myrtille Spentchian, Mélodie Aubart, Cathérine Boileau, Reed E. Pyeritz, Dianna M. Milewicz

    出版 2016
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    Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation

    Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation 由 Solveig Heide, Myrtille Spentchian, Stéphanie Valence, Julien Buratti, Corinne Mach, Élodie Lejeune, Valérie Olin, Marta Massimello, Daphné Lehalle, L. Mouthon, Sandra Whalen, Anne Faudet, Cyril Mignot, Cathérine Garel, Éléonore Blondiaux, Mathilde Lefebvre, Geneviève Quenum-Miraillet, Sandra Chantot‐Bastaraud, Mathieu Milh, Florence Bretelle, Vincent des Portes, Laurent Guibaud, Audrey Putoux, V. Tsatsaris, Marta Spodenkiewic, Valérie Layet, Rodolphe Dard, Laurent Mandelbrot, Agnès Guët, Sébastien Moutton, Magali Gorce, Mathilde Nizon, Marie Vincent, Claire Bénéteau, Marie-Amélie Rocchisanni, Alexandra Benachi, Julien Saada, Tania Attié‐Bitach, Lucie Guilbaud, P Maurice, Stéphanie Friszer, Jean‐Marie Jouannic, Thierry Billette de Villemeur, Marie‐Laure Moutard, Boris Keren, Delphine Héron

    出版 2020
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