Mutation of FGFR2 (cys278phe) in craniolacunia and pansynostosis. [electronic resource]
Producer: 20000725Description: 499-500 p. digitalISSN:- 0022-2593
- Base Sequence
- DNA -- genetics
- DNA Primers -- genetics
- Female
- Humans
- Infant
- Point Mutation
- Receptor Protein-Tyrosine Kinases -- genetics
- Receptor, Fibroblast Growth Factor, Type 2
- Receptors, Fibroblast Growth Factor -- genetics
- Skull -- abnormalities
- Synostosis -- diagnostic imaging
- Tomography, X-Ray Computed
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Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
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