Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Vaux, Keith" or (type any "bookEditor journalEditor issueEditor" and editor="Vaux, Keith") Add to list Conference Paper C3 FOXP1-related intellectual disability syndrome: a recognizable entity Ilse Meerschaut (UGent) , Justine Pètre, Nicole Revencu, Damien Lederer, Milen Vilenov, Thomy de Ravel, Djalila Mekahli, Keith Vaux, Jonathan Sebat, Fadi Hamdan, et al. (2016) Belgian Society of Human Genetics (BeSHG) and the Nederlandse Vereniging voor Humane Genetica (NVHG), 1st Joint meeting, Abstract book. Add to list Conference Paper C3 FOXP1-related intellectual disability syndrome: a recognizable entity Ilse Meerschaut (UGent) , Justine Pètre, Nicole Revencu, Damien Lederer, Milen Vilenov, Thomy de Ravel, Djalila Mekahli, Keith Vaux, Jonathan Sebat, Fadi Hamdan, et al. (2016) BELGIAN JOURNAL OF PAEDIATRICS. 18(1). p.99-99