A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3
- Resource Type
- Source
- Clinical Genetics
- Subject
Fibroblast Growth Factor 9 Male 0301 basic medicine Heterozygote Multiple synostosis syndrome Adolescent fusion of interphalangeal joints Mutation, Missense Short Report 030105 genetics & heredity Biology SYNS FGF9 03 medical and health sciences Short Reports Multiple synostoses syndrome Genetics Humans Receptor, Fibroblast Growth Factor, Type 3 Missense mutation Abnormalities, Multiple Functional studies Genetics (clinical) Medicinsk genetik Radiography stomatognathic diseases Phenotype 030104 developmental biology Synostosis multiple synostosis syndrome Medical Genetics Protein Binding - Language
- English