A patient with novel mutations causing MEN1 and hereditary multiple osteochondroma.

MLA

Remde, Hanna, et al. “A Patient with Novel Mutations Causing MEN1 and Hereditary Multiple Osteochondroma.” Endocrinology, Diabetes & Metabolism Case Reports, vol. 2015, 2015. EBSCOhost, https://doi.org/10.1530/EDM-14-0120.

APA

Remde, H., Kaminsky, E., Werner, M., & Quinkler, M. (2015). A patient with novel mutations causing MEN1 and hereditary multiple osteochondroma. Endocrinology, Diabetes & Metabolism Case Reports, 2015. https://doi.org/10.1530/EDM-14-0120

Chicago

Remde, Hanna, Elke Kaminsky, Mathias Werner, and Marcus Quinkler. 2015. “A Patient with Novel Mutations Causing MEN1 and Hereditary Multiple Osteochondroma.” Endocrinology, Diabetes & Metabolism Case Reports 2015. doi:10.1530/EDM-14-0120.