1. De novo deletions in spinal muscular atrophy: implications for genetic counselling. Issue 1 (January 1997) Authors: Raclin, V; Veber, P S; Bürglen, L; Munnich, A; Melki, J Journal: Journal of medical genetics Issue: Volume 34:Issue 1(1997) Page Start: 86 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes. Issue 3 (March 1992) Authors: Melki, J; Abdelhak, S; Burlet, P; Raclin, V; Kaplan, J; Spiegel, R; Gilgenkrantz, S; Philip, N; Chauvet, M L; Dumez, Y Journal: Journal of medical genetics Issue: Volume 29:Issue 3(1992) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗