Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse. [electronic resource]
Producer: 20051018Description: 3537-48 p. digitalISSN:- 0950-1991
- Acrocephalosyndactylia -- genetics
- Amino Acid Substitution
- Animals
- Bone Development
- Bone and Bones -- abnormalities
- Cartilage -- abnormalities
- Disease Models, Animal
- Exons
- Humans
- Mice
- Mice, Transgenic
- Mutagenesis, Site-Directed
- Polymorphism, Single Nucleotide
- 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, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
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