Alerts
Other content recommended for you
- Prevalence of frailty and pain in hospitalised adult patients in an acute hospital: a protocol for a point prevalence observational study
- Hospitalisation rates for children with intellectual disability or autism born in Western Australia 1983–1999: a population-based cohort study
- Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counselling
- Unexpected Angelman syndrome molecular defect in a girl displaying clinical features of Prader-Willi syndrome
- Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations
- Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region
- Genetic effects on human cognition: lessons from the study of mental retardation syndromes
- Exceptionally mild Angelman syndrome phenotype associated with an incomplete imprinting defect
- Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15
- Validation of intellectual disability coding through hospital morbidity records using an intellectual disability population-based database in Western Australia