1. Genetic heterogeneity of Meckel syndrome. Issue 12 (December 1997) Authors: Roume, J; Ma, H W; Le Merrer, M; Cormier-Daire, V; Girlich, D; Genin, E; Munnich, A Journal: Journal of medical genetics Issue: Volume 34:Issue 12(1997) Page Start: 1003 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Holoprosencephaly-polydactyly ('pseudotrisomy 13') syndrome: a syndrome with features of hydrolethalus and Smith-Lemli-Opitz syndromes. A collaborative multicentre study. Issue 5 (May 1991) Authors: Verloes, A; Aymé, S; Gambarelli, D; Gonzales, M; Le Merrer, M; Mulliez, N; Philip, N; Roume, J Journal: Journal of medical genetics Issue: Volume 28:Issue 5(1991) Page Start: 297 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗