1. "Cataplexy" in Coffin-Lowry syndrome. Issue 8 (August 1998) Authors: Fryns, J P; Smeets, E Journal: Journal of medical genetics Issue: Volume 35:Issue 8(1998) Page Start: 702 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A new centromeric heteromorphism in the short arm of chromosome 20. Issue 9 (September 1988) Authors: Fryns, J P; Kleczkowska, A; Smeets, E; van den Berghe, H Journal: Journal of medical genetics Issue: Volume 25:Issue 9(1988) Page Start: 636 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Profound mental retardation, characteristic facies with midfacial hypoplasia and premature frontotemporal balding, muscular hypotrophy, and small patellae in two unrelated male patients. Issue 4 (April 1993) Authors: Fryns, J P; Thiry, P; Geutjens, J; Smeets, E; Vinken, L; Van den Berghe, H Journal: Journal of medical genetics Issue: Volume 30:Issue 4(1993) Page Start: 319 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Updating the profile of C-terminal MECP2 deletions in Rett syndrome. Issue 4 (12th November 2009) Authors: Bebbington, A; Percy, A; Christodoulou, J; Ravine, D; Ho, G; Jacoby, P; Anderson, A; Pineda, M; Ben Zeev, B; Bahi-Buisson, N; Smeets, E; Leonard, H Journal: Journal of medical genetics Issue: Volume 47:Issue 4(2010) Page Start: 242 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗