APA

Whyte M. P., Totty W. G., Novack D. V., Zhang X., Wenkert D. & Mumm S. (20110817). Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Chicago

Whyte Michael P, Totty William G, Novack Deborah V, Zhang Xiafang, Wenkert Deborah and Mumm Steven. 20110817. Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Harvard

Whyte M. P., Totty W. G., Novack D. V., Zhang X., Wenkert D. and Mumm S. (20110817). Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

MLA

Whyte Michael P, Totty William G, Novack Deborah V, Zhang Xiafang, Wenkert Deborah and Mumm Steven. Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand. : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 20110817.