Search Results (52)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Cation leak through the ATP1A3 pump causes spasticity and intellectual disability. | Academic Article |
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| Considering Decision-Making and Sexuality in Menstrual Suppression of Teens and Young Adults with Intellectual Disabilities. | Academic Article |
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| Phenotypic expansion and variable expressivity in individuals with JARID2-related intellectual disability: A case series. | Academic Article |
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| Hypotonia and intellectual disability without dysmorphic features in a patient with PIGN-related disease. | Academic Article |
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| Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy. | Academic Article |
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| Fragile X Mental Retardation Protein | Concept |
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| Intellectual Disability | Concept |
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| Mental Retardation, X-Linked | Concept |
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| Racial and ethnic disparities in the co-occurrence of intellectual disability and autism: Impact of incorporating measures of adaptive functioning. | Academic Article |
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| Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability. | Academic Article |
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| Use of audio cuing to expand employment opportunities for adolescents with autism spectrum disorders and intellectual disabilities. | Academic Article |
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| Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia. | Academic Article |
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| 15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features. | Academic Article |
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| A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome. | Academic Article |
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| A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. | Academic Article |
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