Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis. [electronic resource]
Producer: 19971006Description: 632-6 p. digitalISSN:- 0022-2593
- Acrocephalosyndactylia -- genetics
- Adult
- Arginine -- genetics
- Child
- Child, Preschool
- Craniosynostoses -- genetics
- Female
- Fibroblast Growth Factors -- genetics
- Humans
- Intellectual Disability -- genetics
- Male
- Mutation
- Proline -- genetics
- Protein-Tyrosine Kinases
- Receptor, Fibroblast Growth Factor, Type 3
- Receptors, Fibroblast Growth Factor -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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