Velocardiofacial syndrome phenotype
Evidence from:
primary |
all sources
Related entities (1)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CNVs | risk_factor_for | Velocardiofacial syndrome | — | 1 |
Mentioned in (9)
Papers in which this entity is mentioned.
- SVXplorer: Three-tier approach to identification of structural variants via sequential recombination of discordant cluster signatures. (2020)
- Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential. (2017)
- Recent genetic findings in schizophrenia and their therapeutic relevance. (2015)
- Atypical cortical gyrification in adolescents with histories of heavy prenatal alcohol exposure. (2015)
- Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013)
- Large-scale objective phenotyping of 3D facial morphology. (2012)
- Catechol-o-methyl transferase (COMT) val158met polymorphism and adolescent cortical development in patients with childhood-onset schizophrenia, their non-psychotic siblings, and healthy controls. (2011)
- Frontoparietal white matter diffusion properties predict mental arithmetic skills in children. (2009)
- Fetal alcohol spectrum disorders and their persisting sequelae in adult life. (2008)
Merged raw entities (2)
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 |
|---|---|---|---|
| velocardiofacial syndrome | phenotype | 9 | 10 |
| vcfs | phenotype | — | — |