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dc.contributor.advisorAldridge, Kristinaeng
dc.contributor.authorGant, Cortaigaeng
dc.contributor.corporatenameUniversity of Missouri--Columbia. School of Medicineeng
dc.date.issued2010eng
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/10355/9166
dc.languageEnglisheng
dc.relation.ispartofcommunityUniversity of Missouri--Columbia. Health Sciences Research Day.eng
dc.rightsOpenAccess.eng
dc.rights.licenseThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.eng
dc.subjectneurological disordereng
dc.subjectbrain developmenteng
dc.subject.FASTApert syndromeeng
dc.titleBrain phenotypes in a mouse model for Apert Syndrome [abstract]eng
dc.typeOthereng


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