@article {3203, title = {Rett syndrome with and without detected MECP2 mutations: An attempt to redefine phenotypes}, journal = {Brain and Development}, volume = {33}, year = {2011}, note = {Cited By (since 1996): 6Export Date: 18 March 2013Source: Scopus}, month = {2011///}, pages = {69 - 76}, url = {http://www.scopus.com/inward/record.url?eid=2-s2.0-78650306582\&partnerID=40\&md5=dbee11e58af80969218350cb4b562c2e}, author = {Temudo, T. and Santos, M. and Ramos, E. and Dias, K. and Vieira, J.P. and Moreira, A. and Calado, E. and Carrilho, I. and Oliveira, G. and Levy, A. and Barbot, C. and Fonseca, M. and Cabral, A. and Cabral, P. and Monteiro, J. and Borges, L. and Gomes, R. and Mira, G. and Aires Pereira, S. and Santos, M. and Fernandes, A. and Epplen, J.T. and Sequeiros, J. and MacIel, P.} }