1. The penta-X syndrome. Issue 5 (October 1980) Authors: Monheit, A; Francke, U; Saunders, B; Jones, K L Journal: Journal of medical genetics Issue: Volume 17:Issue 5(1980) Page Start: 392 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Contribution of molecular analyses in diagnosing Marfan syndrome and type I fibrillinopathies: an international study of 1009 probands. Issue 6 (29th February 2008) Authors: Faivre, L; Collod-Beroud, G; Child, A; Callewaert, B; Loeys, B L; Binquet, C; Gautier, E; Arbustini, E; Mayer, K; Arslan-Kirchner, M; Stheneur, C; Kiotsekoglou, A; Comeglio, P; Marziliano, N; Halliday, D; Beroud, C; Bonithon-Kopp, C; Claustres, M; Plauchu, H; Robinson, P N Journal: Journal of medical genetics Issue: Volume 45:Issue 6(2008) Page Start: 384 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗