Showing 1 - 1 results of 1 for search 'Sandrine Vonwill', query time: 0.05s 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
    Get full text
    Article

Search Tools: