TISSUE SPECIFIC RESPONSES TO ABERRANT FGF SIGNALING IN COMPLEX HEAD PHENOTYPES

BACKGROUND: The role of fibroblast growth factor and receptor (FGF/FGFR) signaling in bone development is well studied, partly because mutations in FGFRs cause human diseases of achondroplasia and FGFR-related craniosynostosis syndromes including Crouzon syndrome. The FGFR2c C342Y mutation is a freq...

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Detalhes bibliográficos
Main Authors: Martínez-Abadías, Neus, Motch, Susan M., Pankratz, Talia L., Wang, Yingli, Aldridge, Kristina, Jabs, Ethylin Wang, Richtsmeier, Joan T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3556393/
https://ncbi.nlm.nih.gov/pubmed/23172727
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.23903
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