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FGF signaling in the developing endochondral skeleton
Mutations in fibroblast growth factor receptors (Fgfrs) are the etiology of many craniosynostosis and chondrodysplasia syndromes in humans. The phenotypes associated with these human syndromes and the phenotypes resulting from targeted mutagenesis in the mouse have defined essential roles for FGF si...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3083241/ https://ncbi.nlm.nih.gov/pubmed/15863035 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cytogfr.2005.02.003 |
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