1. Mutations in the oligophrenin-1 gene (OPHN1) cause X linked congenital cerebellar hypoplasia. Issue 6 (1st June 2003) Authors: Philip, N; Chabrol, B; Lossi, A-M; Cardoso, C; Guerrini, R; Dobyns, W B; Raybaud, C; Villard, L Journal: Journal of medical genetics Issue: Volume 40:Issue 6(2003) Page Start: 441 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Pediatric neuroimaging. (2012) Authors: Barkovich, A. James, 1952-; Raybaud, C Record Type: Book Extent: 1 online resource (1144 pages) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Pediatric neuroimaging. (2018) Authors: Barkovich, A. James, 1952-; Raybaud, C Record Type: Book Extent: 1 online resource View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Pediatric neuroimaging. ([2012]) Other Names: Barkovich, A. James, 1952-; Raybaud, C Record Type: Book Extent: 1 online resource (1143 pages), illustrations View Content: Available online (eLD content is only available in our Reading Rooms) ↗