• Patterns of brain growth in one FGFR2 mouse model for Apert Syndrome 

    Austin, Jordan; Hill, Cheryl A.; Gant, Cortaiga (2010)
    Apert 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 ...