1. Genotype–phenotype correlation in 21 patients with Wolf–Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH). Issue 2 (14th September 2007) Authors: Maas, N M C; Van Buggenhout, G; Hannes, F; Thienpont, B; Sanlaville, D; Kok, K; Midro, A; Andrieux, J; Anderlid, B-M; Schoumans, J; Hordijk, R; Devriendt, K; Fryns, J-P; Vermeesch, J R Journal: Journal of medical genetics Issue: Volume 45:Issue 2(2008) Page Start: 71 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map. Issue 9 (1st September 2004) Authors: Van Buggenhout, G; Melotte, C; Dutta, B; Froyen, G; Van Hummelen, P; Marynen, P; Matthijs, G; de Ravel, T; Devriendt, K; Fryns, J P; Vermeesch, J R Journal: Journal of medical genetics Issue: Volume 41:Issue 9(2004) Page Start: 691 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant. Issue 4 (11th June 2008) Authors: Hannes, F D; Sharp, A J; Mefford, H C; de Ravel, T; Ruivenkamp, C A; Breuning, M H; Fryns, J-P; Devriendt, K; Van Buggenhout, G; Vogels, A; Stewart, H; Hennekam, R C; Cooper, G M; Regan, R; Knight, S J L; Eichler, E E; Vermeesch, J R Journal: Journal of medical genetics Issue: Volume 46:Issue 4(2009) Page Start: 223 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗