Cita APA

Chan, D., Weng, Y. M., Graham, H. K., Sillence, D. O., & Bateman, J. F. (1998). A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasia.

Citación estilo Chicago

Chan, D., Y M. Weng, H K. Graham, D O. Sillence, y J F. Bateman. A Nonsense Mutation in the Carboxyl-terminal Domain of Type X Collagen Causes Haploinsufficiency in Schmid Metaphyseal Chondrodysplasia. 1998.

Cita MLA

Chan, D., et al. A Nonsense Mutation in the Carboxyl-terminal Domain of Type X Collagen Causes Haploinsufficiency in Schmid Metaphyseal Chondrodysplasia. 1998.