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Issue DateTitleAuthor(s)TypeAccess
Aug-2007An explanation for another familial case of Rett syndrome: maternal germline mosaicismVenâncio, Margarida; Santos, Mónica; Pereira, Susana Aires, et al.ArticleOpen access
2008Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardationSantos, Mónica; Yan, Jin; Temudo, Teresa, et al.ArticleRestricted access (UMinho)
2005Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR)Shi, Jinxiu; Shibayama, Akane; Liu, Qiang, et al.ArticleOpen access
Apr-2007Evidence for abnormal early development in a mouse model of Rett syndromeSantos, Mónica; Silva-Fernandes, Anabela; Oliveira, P., et al.ArticleRestricted access (UMinho)
2004Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese originSantos, Mónica; Costa, Maria do Carmo; Rio, Maria Edite, et al.ArticleOpen access
Jun-2007MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patientsCoutinho, Ana M.; Oliveira, Guiomar; Katz, Cécile, et al.ArticleRestricted access (UMinho)
Jan-2009Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patientsSantos, Mónica; Temudo, Teresa; Kay, Teresa, et al.ArticleOpen access
2006Processes : working group reportChatty, Stéphane; Campos, J. Creissac; González, María Paula, et al.Conference paperOpen access
Jan-2011Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypesTemudo, Teresa; Santos, Mónica; Ramos, Elisabete, et al.ArticleOpen access
2008The C677T polymorphism in MTHFR is not associated with migraine in PortugalFerro, Anabela; Castro, Maria-José; Lemos, Carolina, et al.ArticleOpen access