Cite
Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation.
MLA
White, Kenneth E., et al. “Mutations That Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation.” American Journal of Human Genetics, vol. 76, no. 2, Feb. 2005, pp. 361–67. EBSCOhost, https://doi.org/10.1086/427956.
APA
White, K. E., Cabral, J. M., Davis, S. I., Fishburn, T., Evans, W. E., Ichikawa, S., Fields, J., Xijie Yu, Shaw, N. J., McLellan, N. J., McKeown, C., FitzPatrick, D., Kai Yu, Ornitz, D. M., & Econs, M. J. (2005). Mutations that Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation. American Journal of Human Genetics, 76(2), 361–367. https://doi.org/10.1086/427956
Chicago
White, Kenneth E., Jose M. Cabral, Siobhan I. Davis, Tonya Fishburn, Wayne E. Evans, Shoji Ichikawa, Joanna Fields, et al. 2005. “Mutations That Cause Osteoglophonic Dysplasia Define Novel Roles for FGFR1 in Bone Elongation.” American Journal of Human Genetics 76 (2): 361–67. doi:10.1086/427956.