Browsing by Author Barbot, C
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | Type | Access Type |
| 2001 | Clinical and Molecular Findings in Four New Patients Harbouring the mtDNA 8993T C Mutation | Vilarinho, L; Carrozzo, R; Barbot, C; Calado, E; Tessa, A; Dionisi-Vici, C; Guimarães, A; Santorelli, FM | article |  |
| Dec-2008 | LAMA2 Gene Analysis in a Cohort of 26 Congenital Muscular Dystrophy Patients | Oliveira, J; Santos, R; Soares-Silva, I; Jorge, P; Vieira, E; Oliveira, ME; Moreira, A; Coelho, T; Ferreira, JC; Fonseca, MJ; Barbosa, C; Prats, J; Aríztegui, ML; Martins, ML; Moreno, T; Heinimann, K; Barbot, C; Pascual-Pascual, SI; Cabral, A; Fineza, I; Santos, M; Bronze-da-Rocha, E | article | |
| 2011 | Rett Syndrome With and Without Detected MECP2 Mutations: an Attempt to Redefine Phenotypes | Temudo, T; Santos, M; Ramos, E; Dias, K; Vieira, JP; Moreira, A; Calado, E; Carrilho, I; Oliveira, G; Levy, A; Barbot, C; Fonseca, M; Cabral, A; Cabral, P; Monteiro, J; Borges, L; Gomes, R; Mira, G; Pereira, SA; Santos, M; Fernandes, A; Epplen, JT; Sequeiros, J; Maciel, P | article | |
