Search Results (84)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| New Frontier: The First Year of an Adult Neurodevelopmental Disabilities Clinic. | Academic Article |
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| CO Leadership & Education in Neurodevelopmental Disabilities | Grant |
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| Sanders, Jessica | Person |
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| Understanding and Using Neurocognitive Assessment Results in Children with Neurodevelopmental Disabilities. In M L Batshaw, N Roizen, G Lotrecchiano (Eds). Children with Disabilities, 7th Edition. Baltimore: Brookes Publishing | Academic Article |
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| De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype. | Academic Article |
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| Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3. | Academic Article |
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| Johnson, Susan | Person |
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| De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay. | Academic Article |
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| The Causal Effect of Part C Early Intervention on Low-income and Very Low Birth Weight Infants | Grant |
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| CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. | Academic Article |
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| Project TENDR: Targeting Environmental Neuro-Developmental Risks The TENDR Consensus Statement. | Academic Article |
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| Cole, Jordan | Person |
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| Haploinsufficiency as a disease mechanism in GNB1-associated neurodevelopmental disorder. | Academic Article |
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| Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report. | Academic Article |
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| CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity. | Academic Article |
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