Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family.
- Resource Type
- Article
- Source
- Molecular Syndromology; Mar2017, Vol. 8 Issue 2, p93-97, 5p, 1 Color Photograph, 1 Black and White Photograph, 1 Chart, 1 Graph
- Subject
- Language
- ISSN
- 16618769