Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4. [electronic resource]
Producer: 19981006Description: 76-9 p. digitalISSN:- 1096-7192
- Acrocephalosyndactylia -- genetics
- Arginine
- Base Sequence
- Child
- Craniosynostoses -- genetics
- Deoxyribonucleases, Type II Site-Specific
- Genetic Testing
- Humans
- Point Mutation
- Polymerase Chain Reaction
- Polymorphism, Single-Stranded Conformational
- Proline
- Protein-Tyrosine Kinases
- Receptor Protein-Tyrosine Kinases -- genetics
- Receptor, Fibroblast Growth Factor, Type 1
- Receptor, Fibroblast Growth Factor, Type 2
- Receptor, Fibroblast Growth Factor, Type 3
- Receptor, Fibroblast Growth Factor, Type 4
- Receptors, Fibroblast Growth Factor -- genetics
- Sequence Homology, Amino Acid
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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