Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes - Temudo, T.; Santos, M.; Ramos, E.; Dias, K.; Vieira, J.P.; Moreira, A.; Calado, E.; Carrilho, I.; Oliveira, G.; Levy, A.; Barbot, C.; Fonseca, M.; et al. (Brain and Development, 2011)
Cited By (since 1996): 6Export Date: 18 March 2013Source: Scopus