Search Results (106)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
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| Sanders, Jessica | Person |
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| De novo loss-of-function variant in PTDSS1 is associated with developmental delay. | 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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| A systematic review of sensory-based treatments for children with disabilities. | Academic Article |
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| FOLLOW-UP OF FAMILIES IN EARLY PREVENTIVE INTERVENTION | Grant |
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| FOLLOW-UP OF FAMILIES IN EARLY PREVENTIVE INTERVENTION | Grant |
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| Larson, Austin | Person |
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| Behavioral and Neural Outcomes of a New Executive Function Treatment for Transition-Age Youth with ASD | Grant |
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| The clinical and genetic spectrum of inherited glycosylphosphatidylinositol deficiency disorders. | Academic Article |
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| Novel de novo variant in EBF3 is likely to impact DNA binding in a patient with a neurodevelopmental disorder and expanded phenotypes: patient report, in silico functional assessment, and review of published cases. | Academic Article |
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| Gracie, Sara | Person |
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| Olds, David | Person |
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| Brief Report: The ADOS Calibrated Severity Score Best Measures Autism Diagnostic Symptom Severity in Pre-School Children. | Academic Article |
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| Novel NR2F1 variants likely disrupt DNA binding: molecular modeling in two cases, review of published cases, genotype-phenotype correlation, and phenotypic expansion of the Bosch-Boonstra-Schaaf optic atrophy syndrome. | Academic Article |
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| Interstitial deletion of (17)(p11.2p11.2) in nine patients. | Academic Article |
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