APA (7th ed.) Citation

N, P., Jr, A. J., A, M., AV, E., J, M., OA, I., . . . Jr, C. W. (2006). Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism. Proceedings of the National Academy of Sciences of the United States of America, 103(16), 6281. https://doi.org/10.1073/pnas.0600962103

Chicago Style (17th ed.) Citation

N, Pitteloud, et al. "Mutations in Fibroblast Growth Factor Receptor 1 Cause Both Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism." Proceedings of the National Academy of Sciences of the United States of America 103, no. 16 (2006): 6281. https://doi.org/10.1073/pnas.0600962103.

MLA (9th ed.) Citation

N, Pitteloud, et al. "Mutations in Fibroblast Growth Factor Receptor 1 Cause Both Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism." Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 16, 2006, p. 6281, https://doi.org/10.1073/pnas.0600962103.