Search Results - Vonwill, Sandrine

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  1. 1
    Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth

    Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth by Jeanne, Médéric, Vuillaume, Marie-Laure, Ung, Dévina C., Vancollie, Valerie E., Wagner, Christel, Collins, Stephan C., Vonwill, Sandrine, Haye, Damien, Chelloug, Nora, Pfundt, Rolph, Kummeling, Joost, Moizard, Marie-Pierre, Marouillat, Sylviane, Kleefstra, Tjitske, Yalcin, Binnaz, Laumonnier, Frédéric, Toutain, Annick

    Published in Human genetics
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    Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders

    Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders by Bitar, Tania, Hleihel, Walid, Marouillat, Sylviane, Vonwill, Sandrine, Vuillaume, Marie‐Laure, Soufia, Michel, Vourc'h, Patrick, Laumonnier, Frederic, Andres, Christian R.

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