1. SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype. Issue 7 (14th April 2009) Authors: Pasmant, E; Sabbagh, A; Hanna, N; Masliah-Planchon, J; Jolly, E; Goussard, P; Ballerini, P; Cartault, F; Barbarot, S; Landman-Parker, J; Soufir, N; Parfait, B; Vidaud, M; Wolkenstein, P; Vidaud, D; France, R N F Journal: Journal of medical genetics Issue: Volume 46:Issue 7(2009) Page Start: 425 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗