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dc.contributor.advisorAldridge, Kristinaeng
dc.contributor.authorAustin, Jordaneng
dc.contributor.authorHill, Cheryl A.eng
dc.contributor.authorGant, Cortaigaeng
dc.contributor.corporatenameUniversity of Missouri--Columbia. School of Medicineeng
dc.contributor.meetingnameHealth Sciences Research Day (2010 : University of Missouri)eng
dc.date.issued2010eng
dc.description.abstractApert syndrome is a disorder associated with craniosynostosis resulting from one of two mutations in Fibroblast Growth Factor Receptor 2 (FGFR2). Individuals with Apert syndrome demonstrate brain dysmorphology, often associated with cognitive deficits. In this study, micro magnetic resonance images of the brain of FGFR2+/P253R mice and their wildtype littermates were acquired at two ages, P0 (newborn) and P2 (two days old). Fifteen landmarks on the brain surface were collected to compare growth patterns in the morphological phenotypes of the brain.eng
dc.description.sponsorship"Work supported by NIDCR R01 DE018500"eng
dc.format.extent2 files (1 page, 1 poster)eng
dc.identifier.urihttp://hdl.handle.net/10355/9384
dc.languageEnglisheng
dc.relation.ispartofcommunityUniversity of Missouri--Columbia. Health Sciences Research Dayeng
dc.rightsOpenAccess.eng
dc.rights.licenseThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.eng
dc.subjectbrain developmenteng
dc.subjectcongenital disorderseng
dc.subject.lcshApert syndromeeng
dc.subject.lcshBrain -- Growtheng
dc.subject.lcshCorpus callosumeng
dc.titlePatterns of brain growth in one FGFR2 mouse model for Apert Syndromeeng
dc.typeOthereng


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