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Cation leak through the ATP1A3 pump causes spasticity and intellectual disability.Academic Article Why?
Considering Decision-Making and Sexuality in Menstrual Suppression of Teens and Young Adults with Intellectual Disabilities.Academic Article Why?
Phenotypic expansion and variable expressivity in individuals with JARID2-related intellectual disability: A case series.Academic Article Why?
Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease.Academic Article Why?
Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy.Academic Article Why?
Fragile X Mental Retardation ProteinConcept Why?
Intellectual DisabilityConcept Why?
Mental Retardation, X-LinkedConcept Why?
Racial and ethnic disparities in the co-occurrence of intellectual disability and autism: Impact of incorporating measures of adaptive functioning.Academic Article Why?
Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability.Academic Article Why?
Use of audio cuing to expand employment opportunities for adolescents with autism spectrum disorders and intellectual disabilities.Academic Article Why?
Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.Academic Article Why?
15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features.Academic Article Why?
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome.Academic Article Why?
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.Academic Article Why?
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