2010
Hill C, Vaddi S, Moffitt A, Kane A, Marsh J, Panchal J, Richtsmeier J, Aldridge K. 2010. Intracranial volume and whole brain volume in infants with unicoronal craniosynostosis. Cleft palate-Craniofacial Journal . 2010 Aug 10.
N Martínez-Abadías, C Percival, K Aldridge, CA Hill, T Ryan, S Sirivunnabood, Y Wang, EW Jabs, JT Richtsmeier. 2010. Beyond the closed suture in Apert syndrome mouse models: evidence of primary effects of FGFR2 signaling on facial shape at birth. Dev Dyn . 239:3058-3071. https://doi.org/10.1002/dvdy.22414
CC Roseman, KE Willmore, J Rogers, C Hildebolt, BE Sadler, JT Richtsmeier, JM Cheverud. 2010. Genetic and environmental contributions to variation in baboon cranial morphology. Amer. J. Phys. Anthropol . 143:1-12. https://doi.org/10.1002/ajpa.21341
HeuzéY, SA Boyadjiev, JL Marsh, AA Kane, E Cherkez, JE Boggan, JT Richtsmeier. 2010. New insights into the relationship between suture closure and craniofacial dysmorphology in sagittal nonsyndromic craniosynostosis. J Anat . 217:85-96.https://doi.org/10.1111/j.1469-7580.2010.01258.x
Wang Y, M Sun, VL Uhlhorn, X Zhou, I Peter, N Martinez-Abadias, CA Hill, CJ Percival, JT Richtsmeier, DL Huso, EW Jabs. 2010. Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+/P253R mice. BMC Developmental Biology. 10(22). https://doi.org/10.1186/1471-213X-10-22
Aldridge, K, CA Hill, JR Austin, C Perival, N Martinez-Abadias, T Neuberger, Y Wang, EW Jabs, JT Richtsmeier. 2010. Brain phenotypes in two FGFR2 mouse models for Apert syndrome. Devel Dyn. 239: 987-997. https://doi.org/10.1002/dvdy.22218
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