APA Alıntı

Mannstadt, M., Bertrand, G., Muresan, M., Weryha, G., Leheup, B., Pulusani, S. R., . . . Silve, C. (2008). Dominant-Negative GCMB Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism. The Endocrine Society.

Chicago Stili Alıntı

Mannstadt, Michael, Guylène Bertrand, Mihaela Muresan, Georges Weryha, Bruno Leheup, Sirish R. Pulusani, Bernard Grandchamp, Harald Jüppner, ve Caroline Silve. Dominant-Negative GCMB Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism. The Endocrine Society, 2008.

MLA Alıntı

Mannstadt, Michael, et al. Dominant-Negative GCMB Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism. The Endocrine Society, 2008.