NELE BOCKAERT 1 – 3 of 3 publications Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Filter publications Download search results Subscribe to news feed Add to list Journal Article A1 FOXP1-related intellectual disability syndrome : a recognisable entity Ilse Meerschaut (UGent) , Daniel Rochefort, Nicole Revençu, Justine Pètre, Christina Corsello, Guy A Rouleau, Fadi F Hamdan, Jacques L Michaud, Jenny Morton, Jessica Radley, et al. (2017) JOURNAL OF MEDICAL GENETICS. 54(9). p.613-623 Add to list Conference Paper C3 FOXP1-related intellectual disability syndrome : a recognizable entity Ilse Meerschaut (UGent) , J Pètre, N Revencu, NELE BOCKAERT, Ann Oostra (UGent) , Olivier Vanakker (UGent) , M Velinov, TJ de Ravel, D Mekahli, KK Vaux, et al. (2016) Eur. J. Hum. Genet.. In EUROPEAN JOURNAL OF HUMAN GENETICS 24(E-suppl. 1). p.161-161 Add to list Journal Article A1 Two siblings with early presentation of Vanishing White Matter disease NELE BOCKAERT, M VAN DER KNAAP, C VAN DEN BROECKE, Helene Verhelst (UGent) , M LAMMENS and Rudy Van Coster (UGent) (2004) ACTA NEUROLOGICA BELGICA. 104(1). p.43-43