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dc.contributor.advisorAldridge, Kristinaeng
dc.contributor.authorGant, Cortaigaeng
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.eng
dc.identifier.urihttp://hdl.handle.net/10355/9166eng
dc.relation.ispartof2010 Health Sciences Research Day (MU)eng
dc.relation.ispartofcommunityUniversity of Missouri-Columbia. Health Sciences Research Day.eng
dc.subjectneurological disordereng
dc.subjectbrain developmenteng
dc.titleBrain phenotypes in a mouse model for Apert Syndrome [abstract]eng
dc.typeOthereng


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