1. A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism. Issue 12 (24th September 2014) Authors: De Wolf, Veerle; Crepel, An; Schuit, Frans; van Lommel, Leentje; Ceulemans, Berten; Steyaert, Jean; Seuntjens, Eve; Peeters, Hilde; Devriendt, Koen Journal: American journal of medical genetics Issue: Volume 164:Issue 12(2014.) Page Start: 3035 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association of CDH11 with non‐syndromic ASD. Issue 5 (19th May 2014) Authors: Crepel, An; De Wolf, Veerle; Brison, Nathalie; Ceulemans, Berten; Walleghem, Didier; Peuteman, Gilian; Lambrechts, Diether; Steyaert, Jean; Noens, Ilse; Devriendt, Koen; Peeters, Hilde Journal: American journal of medical genetics Issue: Volume 165:Issue 5(2014) Page Start: 391 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example. Issue 11 (10th October 2013) Authors: De Wolf, Veerle; Brison, Nathalie; Devriendt, Koenraad; Peeters, Hilde Journal: American journal of medical genetics Issue: Volume 161:Issue 11(2013:Nov.) Page Start: 2846 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗