Brain Phenotypes in Two FGFR2 Mouse Models for Apert Syndrome

Apert syndrome (AS) is one of at least nine disorders considered members of the fibroblast growth factor receptor (FGFR) -1, -2, and -3–related craniosynostosis syndromes. Nearly 100% of individuals diagnosed with AS carry one of two neighboring mutations on Fgfr2. The cranial phenotype associated w...

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Main Authors: Aldridge, Kristina, Hill, Cheryl A., Austin, Jordan R., Percival, Christopher, Martinez-Abadias, Neus, Neuberger, Thomas, Wang, Yingli, Jabs, Ethylin Wang, Richtsmeier, Joan T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2829947/
https://ncbi.nlm.nih.gov/pubmed/20077479
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.22218
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