1. Novel FOXG1 mutations associated with the congenital variant of Rett syndrome. Issue 1 (2nd July 2009) Authors: Mencarelli, M A; Spanhol-Rosseto, A; Artuso, R; Rondinella, D; De Filippis, R; Bahi-Buisson, N; Nectoux, J; Rubinsztajn, R; Bienvenu, T; Moncla, A; Chabrol, B; Villard, L; Krumina, Z; Armstrong, J; Roche, A; Pineda, M; Gak, E; Mari, F; Ariani, F; Renieri, A Journal: Journal of medical genetics Issue: Volume 47:Issue 1(2010) Page Start: 49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗