1. 3M dwarfism: a study of two further sibs. Issue 9 (September 1989) Authors: Feldmann, M; Gilgenkrantz, S; Parisot, S; Zarini, G; Marchal, C Journal: Journal of medical genetics Issue: Volume 26:Issue 9(1989) Page Start: 583 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Features of Turner's and DiGeorge's syndromes with X;22 translocation. Issue 12 (December 1990) Authors: Gilgenkrantz, S; Teboul, M Journal: Journal of medical genetics Issue: Volume 27:Issue 12(1990) Page Start: 791 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Partial proximal trisomy of the long arm of chromosome 5 (q13 leads to q22) resulting from maternal insertion der ins (10;5). Issue 6 (December 1981) Authors: Gilgenkrantz, S; Dulucq, P; Bresson, J L; Gouget, A; Pernot, C; Gregoire, M J Journal: Journal of medical genetics Issue: Volume 18:Issue 6(1981) Page Start: 465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. 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) ↗