deafness phenotype
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (7)
Papers in which this entity is mentioned.
- Heritability and genomics of gene expression in peripheral blood. (2014)
- Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. (2010)
- Genome-wide association studies in ADHD. (2009)
- Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)
- SNPs3D: candidate gene and SNP selection for association studies. (2006)
- Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis. (2005)
- Neomycin-induced hair cell death and rapid regeneration in the lateral line of zebrafish (Danio rerio). (2003)
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 |
|---|---|---|---|
| deafness | phenotype | 7 | 7 |