Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. [electronic resource]
Producer: 19950106Description: 98-103 p. digitalISSN:- 1061-4036
- Base Sequence
- Chromosomes, Human, Pair 10
- Craniofacial Dysostosis -- genetics
- Exons
- Female
- Humans
- Lod Score
- Male
- Molecular Sequence Data
- Mutation
- Pedigree
- Polymorphism, Single-Stranded Conformational
- Receptor Protein-Tyrosine Kinases -- genetics
- Receptor, Fibroblast Growth Factor, Type 2
- Receptors, Fibroblast Growth Factor -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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