[-] Show simple item record

dc.contributor.advisorAldridge, Kristinaen_US
dc.contributor.authorGant, Cortaiga
dc.date.issued2010-11eng
dc.description.abstractApert 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.identifier.urihttp://hdl.handle.net/10355/9166
dc.relation.ispartof2010 Health Sciences Research Day (MU)en_US
dc.relation.ispartofcommunityUniversity of Missouri-Columbia. Health Sciences Research Day.
dc.subjectneurological disorderen_US
dc.subjectbrain developmenten_US
dc.titleBrain phenotypes in a mouse model for Apert Syndrome [abstract]en_US
dc.typeOtheren_US


Files in this item

[PDF]

This item appears in the following Collection(s)

[-] Show simple item record