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    Brain phenotypes in a mouse model for Apert Syndrome [abstract]

    Gant, Cortaiga
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    [PDF] BrainPhenotypesMouseModel.pdf (223.4Kb)
    Date
    2010
    Contributor
    University of Missouri--Columbia. School of Medicine
    Format
    Abstract
    Metadata
    [+] Show full item record
    Abstract
    Apert Syndrome (AS) is one of several fibroblast growth factor receptor (FGFR) related craniosynostosis syndromes. Individuals with AS display craniofacial dysmorphology and a constellation of central nervous system anomalies. In this study we present quantitative comparisons of brain phenotypes in a mouse model for Apert syndrome, the Fgfr2+/S252W mouse.
    URI
    http://hdl.handle.net/10355/9166
    Rights
    OpenAccess.
    This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.
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