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Showing 1 - 1 results of 1 for search 'Sandrine Vonwill', query time: 0.02s Refine Results
  1. 1
    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 Tania Bitar, Walid Hleihel, Sylviane Marouillat, Sandrine Vonwill, Marie‐Laure Vuillaume, Michel Soufia, Patrick Vourc'h, Frederic Laumonnier, Christian R. Andres
    Published 2019-08-01
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