Search Results (212)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
|---|
| A new neurodevelopmental disorder linked to heterozygous variants in UNC79. | Academic Article |
Why?
|
| Common molecular mechanisms of SLC6A1 variant-mediated neurodevelopmental disorders in astrocytes and neurons. | Academic Article |
Why?
|
| Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. | Academic Article |
Why?
|
| Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders. | Academic Article |
Why?
|
| Maternal Psychiatric Conditions, Treatment With Selective Serotonin Reuptake Inhibitors, and Neurodevelopmental Disorders. | Academic Article |
Why?
|
| Preconception and Prenatal Nutrition and Neurodevelopmental Disorders: A Systematic Review and Meta-Analysis. | Academic Article |
Why?
|
| AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders. | Academic Article |
Why?
|
| Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders. | Academic Article |
Why?
|
| Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders. | Academic Article |
Why?
|
| The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder. | Academic Article |
Why?
|
| De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder. | Academic Article |
Why?
|
| Cole, Jordan | Person |
Why?
|
| Early Life Experience and Neurodevelopmental Disorders | Grant |
Why?
|
| Astrocytes in Neural Circuits: Key Factors in Synaptic Regulation and Potential Targets for Neurodevelopmental Disorders. | Academic Article |
Why?
|
| Current knowledge of SLC6A1-related neurodevelopmental disorders. | Academic Article |
Why?
|