1. Clinical, molecular, and genotype–phenotype correlation studies from 25 cases of oral–facial–digital syndrome type 1: a French and Belgian collaborative study. Issue 1 (5th January 2006) Authors: Thauvin-Robinet, C; Cossée, M; Cormier-Daire, V; Van Maldergem, L; Toutain, A; Alembik, Y; Bieth, E; Layet, V; Parent, P; David, A; Goldenberg, A; Mortier, G; Héron, D; Sagot, P; Bouvier, A M; Huet, F; Cusin, V; Donzel, A; Devys, D; Teyssier, J R Journal: Journal of medical genetics Issue: Volume 43:Issue 1(2006) Page Start: 54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation. Issue 11 (November 1992) Authors: Heitz, D; Devys, D; Imbert, G; Kretz, C; Mandel, J L Journal: Journal of medical genetics Issue: Volume 29:Issue 11(1992) Page Start: 794 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗