1. Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family. Issue 8 (August 1994) Authors: de Die-Smulders, C E; Höweler, C J; Mirandolle, J F; Brunner, H G; Hovers, V; Brüggenwirth, H; Smeets, H J; Geraedts, J P Journal: Journal of medical genetics Issue: Volume 31:Issue 8(1994) Page Start: 595 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Arthrogryposis, ophthalmoplegia, and retinopathy: confirmation of a new type of arthrogryposis. Issue 1 (January 1993) Authors: Schrander-Stumpel, C T; Höweler, C J; Reekers, A D; De Smet, N M; Hall, J G; Fryns, J P Journal: Journal of medical genetics Issue: Volume 30:Issue 1(1993) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Intestinal pseudo-obstruction in myotonic dystrophy. Issue 11 (November 1992) Authors: Brunner, H G; Hamel, B C; Rieu, P; Höweler, C J; Peters, F T Journal: Journal of medical genetics Issue: Volume 29:Issue 11(1992) Page Start: 791 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗
5. Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports. Issue 5 (May 1979) Authors: Pearse, R G; Höweler, C J Journal: Archives of disease in childhood Issue: Volume 54:Issue 5(1979) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Paternal transmission of congenital myotonic dystrophy. Issue 11 (November 1997) Authors: de Die-Smulders, C E; Smeets, H J; Loots, W; Anten, H B; Mirandolle, J F; Geraedts, J P; Höweler, C J Journal: Journal of medical genetics Issue: Volume 34:Issue 11(1997) Page Start: 930 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗