Hand stereotypies: Lessons from the Rett Syndrome Natural History Study

Severity assessment in CDKL5 deficiency disorder

Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome

The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2

Behavioral profiles in Rett syndrome: Data from the Natural History Study

The course of awake breathing disturbances across the lifespan in Rett syndrome

When Rett syndrome is due to genes other than MECP2

Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors

Assessment of caregiver inventory for Rett syndrome

Longitudinal course of epilepsy in Rett syndrome and related disorders

From function to phenotype: impaired DNA binding and clustering correlates with clinical severity in males with missense mutations in MECP2

Loss of MeCP2 causes urological dysfunction and contributes to death by kidney failure in mouse models of Rett syndrome