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

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

Please use this identifier to cite or link to this item: http://hdl.handle.net/10355/9166

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dc.contributor.advisor Aldridge, Kristina en_US
dc.contributor.author Gant, Cortaiga
dc.date.accessioned 2010-12-06T14:31:44Z
dc.date.available 2010-12-06T14:31:44Z
dc.date.issued 2010-11-11
dc.identifier.uri http://hdl.handle.net/10355/9166
dc.description.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. en_US
dc.language.iso en_US en_US
dc.relation.ispartof 2010 Health Sciences Research Day (MU) en_US
dc.subject neurological disorder en_US
dc.subject brain development en_US
dc.title Brain phenotypes in a mouse model for Apert Syndrome [abstract] en_US
dc.type Other en_US
dc.relation.ispartofcommunity University of Missouri-Columbia. Health Sciences Research Day.


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