neurodevelopmental phenotype phenotype
Evidence from:
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Mentioned in (3)
Papers in which this entity is mentioned.
- Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
- 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
- Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013)
Merged raw entities (1)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| neurodevelopmental phenotype | phenotype | 3 | 4 |