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Issue Date	Title / Author(s) / Citation	File
2009	Functional Charaterization of a Novel FGFR2 Mutation, E731K, in Craniosynostosis 박정현	link
2021-02	Investigation of developmental mechanisms and establishment of treatment strategies: 3D morphometric analysis of midface anomalies in a mouse model of Apert syndrome 김봉수	view file link
2022-04	Excessive osteoclast activation by osteoblast paracrine factor RANKL is a major cause of the abnormal long bone phenotype in Apert syndrome model mice Shin, Hye-Rim; Kim, Bong-Soo; Kim, Hyun-Jung; Yoon, Heein; Kim, Woo-Jin; Choi, Je-Yong; Ryoo, Hyun-Mo Journal of Cellular Physiology, Vol.237 No.4, pp.2155-2168	DOI