1. MASA syndrome (a form of complicated spastic paraplegia) and X linked hydrocephalus: variable expression of the same mutation at Xq28? Call for families. Issue 3 (March 1992) Authors: Schrander-Stumpel, C; Fryns, J; Cassiman, J J; Legius, E; Spaepen, A; Höweler, C J Journal: Journal of medical genetics Issue: Volume 29:Issue 3(1992) Page Start: 215 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Neurofibromatosis type 1 in childhood: correlation of MRI findings with intelligence. Issue 6 (December 1995) Authors: Legius, E; Descheemaeker, M J; Steyaert, J; Spaepen, A; Vlietinck, R; Casaer, P; Demaerel, P; Fryns, J P Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 59:Issue 6(1995) Page Start: 638 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The variable clinical spectrum and mental prognosis of the acrocallosal syndrome. Issue 3 (March 1991) Authors: Fryns, J P; Spaepen, A; Grubben, C; van den Berghe, H; Casaer, P Journal: Journal of medical genetics Issue: Volume 28:Issue 3(1991) Page Start: 214 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28. Issue 6 (June 1991) Authors: Fryns, J P; Spaepen, A; Cassiman, J J; van den Berghe, H Journal: Journal of medical genetics Issue: Volume 28:Issue 6(1991) Page Start: 429 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗