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="Vandeweyer, G" or (type exact bookEditor and editor="Vandeweyer, G") Add to list Journal Article A1 Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencing C Helsmoortel, G Vandeweyer, P Ordoukhanian, Filip Van Nieuwerburgh (UGent) , N Van der Aa and RF Kooy (2015) CLINICAL GENETICS. 88(2). p.140-148 Add to list Conference Paper C3 Mutation of the iron-sulfur cluster assembly IBA57 gene causes lethal myopathy and encephalopathy N Ajit Bolar, Arnaud Vanlander (UGent) , C Wilbrecht, Nathalie Van der Aa, Joél Smet (UGent) , Boel De Paepe (UGent) , G Vandeweyer, F Kooy, François Eyskens, Elien De Latter (UGent) , et al. (2013) EUROPEAN JOURNAL OF HUMAN GENETICS. 21(suppl. 2). p.30-30 Add to list Journal Article A1 open access Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome BWM van Bon, HC Mefford, Björn Menten (UGent) , DA Koolen, AJ Sharp, WM Nillesen, JW Innis, TJL de Ravel, CL Mercer, M Fichera, et al. (2009) JOURNAL OF MEDICAL GENETICS. 46(8). p.511-523