1. A Familial Heterozygous Null Mutation of MET in Autism Spectrum Disorder2. Issue 5 (6th June 2014) Authors: Lambert, Nelle; Wermenbol, Vanessa; Pichon, Bruno; Acosta, Sandra; van den Ameele, Jelle; Perazzolo, Camille; Messina, Diana; Musumeci, Maria‐Franca; Dessars, Barbara; De Leener, Anne; Abramowicz, Marc; Vilain, Catheline Journal: Autism research Issue: Volume 7:Issue 5(2014:Oct.) Page Start: 617 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Corpus callosum thinning in autosomal dominant hereditary spastic paraplegia associated with a novel TUBβ4A mutation. Issue 4 (28th July 2020) Authors: Lamartine S. Monteiro, Marta; Vandernoot, Isabelle; Desmyter, Laurence; Wermenbol, Vanessa; Naeije, Gilles; Remiche, Gauthier Journal: Clinical genetics Issue: Volume 98:Issue 4(2020) Page Start: 416 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗