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Quoted phrase not found in phrase index: "Rett syndrome, congenital variant"
Page 1
Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.
Hoffbuhr KC, Moses LM, Jerdonek MA, Naidu S, Hoffman EP. Hoffbuhr KC, et al. Ment Retard Dev Disabil Res Rev. 2002;8(2):99-105. doi: 10.1002/mrdd.10026. Ment Retard Dev Disabil Res Rev. 2002. PMID: 12112735 Review.
Rett syndrome is a neurodevelopmental disorder of early postnatal brain growth in girls. ...Nonrandom patterns of X-inactivation may also contribute to the clinical variability often seen in girls with Rett syndrome. The spectrum of clinical …
Rett syndrome is a neurodevelopmental disorder of early postnatal brain growth in girls. ...Nonrandom patterns of X-inactivati …
Oxidative stress in Rett syndrome: natural history, genotype, and variants.
Leoncini S, De Felice C, Signorini C, Pecorelli A, Durand T, Valacchi G, Ciccoli L, Hayek J. Leoncini S, et al. Redox Rep. 2011;16(4):145-53. doi: 10.1179/1351000211Y.0000000004. Redox Rep. 2011. PMID: 21888765 Free PMC article. Clinical Trial.
OBJECTIVES: Rett syndrome (RTT) is an X-linked autism spectrum disorder caused by mutations in the MeCP2 gene in the great majority of cases. ...Higher OS markers were observed in typical RTT and early seizure variant as compared with the preserved speech and …
OBJECTIVES: Rett syndrome (RTT) is an X-linked autism spectrum disorder caused by mutations in the MeCP2 gene in the great maj …