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 exact 050870D8-F0EE-11E1-A9DE-61C894A0A6B4 cql: author exact F8FBA0DA-F0ED-11E1-A9DE-61C894A0A6B4 Add to list Journal Article A1 open access A reassessment of copy number variations in congenital heart defects : picturing the whole genome Ilse Meerschaut (UGent) , Sarah Vergult (UGent) , Annelies Dheedene (UGent) , Björn Menten (UGent) , Katya De Groote (UGent) , Hans De Wilde (UGent) , Laura Muiño Mosquera (UGent) , Joseph Panzer (UGent) , Kristof Vandekerckhove (UGent) , Paul Coucke (UGent) , et al. (2021) GENES. 12(7). 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