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

dc.contributor.advisor	Aldridge, Kristina	eng
dc.contributor.author	Gant, Cortaiga	eng
dc.contributor.corporatename	University of Missouri--Columbia. School of Medicine	eng
dc.contributor.meetingname	Health Sciences Research Day (2010 : University of Missouri)	eng
dc.date.issued	2010	eng
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.	eng
dc.format.extent	1 page	eng
dc.identifier.uri	http://hdl.handle.net/10355/9166
dc.language	English	eng
dc.relation.ispartofcommunity	University of Missouri--Columbia. Health Sciences Research Day	eng
dc.rights	OpenAccess.	eng
dc.rights.license	This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.	eng
dc.subject	neurological disorder	eng
dc.subject	brain development	eng
dc.subject.FAST	Apert syndrome	eng
dc.title	Brain phenotypes in a mouse model for Apert Syndrome [abstract]	eng
dc.type	Abstract	eng

2010 Health Sciences Research Day (MU)
Poster presentation abstracts for 2010 Health Sciences Research Day.