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

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

Please use this identifier to cite or link to this item: http://hdl.handle.net/10355/9166

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Title: Brain phenotypes in a mouse model for Apert Syndrome [abstract]
Author: Gant, Cortaiga
Keywords: neurological disorder
brain development
Date: 2010-11-11
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.
URI: http://hdl.handle.net/10355/9166

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