APA (7th ed.) Citation

N, P., A, M., R, Q., Jr, A. J., AA, D., L, P., . . . Jr, C. W. (2006). Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. Molecular and cellular endocrinology, 254-255, 60. https://doi.org/10.1016/j.mce.2006.04.021

Chicago Style (17th ed.) Citation

N, Pitteloud, et al. "Mutations in Fibroblast Growth Factor Receptor 1 Cause Kallmann Syndrome with a Wide Spectrum of Reproductive Phenotypes." Molecular and Cellular Endocrinology 254-255 (2006): 60. https://doi.org/10.1016/j.mce.2006.04.021.

MLA (9th ed.) Citation

N, Pitteloud, et al. "Mutations in Fibroblast Growth Factor Receptor 1 Cause Kallmann Syndrome with a Wide Spectrum of Reproductive Phenotypes." Molecular and Cellular Endocrinology, vol. 254-255, 2006, p. 60, https://doi.org/10.1016/j.mce.2006.04.021.