1. Myhre syndrome: new reports, review, and differential diagnosis. Issue 7 (1st July 2003) Authors: Burglen, L; Héron, D; Moerman, A; Dieux-Coeslier, A; Bourguignon, J-P; Bachy, A; Carel, J-C; Cormier-Daire, V; Manouvrier, S; Verloes, A Journal: Journal of medical genetics Issue: Volume 40:Issue 7(2003) Page Start: 546 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome. Issue 10 (1st October 1999) Authors: Manouvrier-Hanu, S; Amiel, J; Jacquot, S; Merienne, K; Moerman, A; Coëslier, A; Labarriere, F; Vallée, L; Croquette, M F; Hanauer, A Journal: Journal of medical genetics Issue: Volume 36:Issue 10(1999) Page Start: 775 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗