APA (7th ed.) Citation

Pitteloud, N., Meysing, A., Quinton, R., Acierno, J. S., Dwyer, A. A., Plummer, L., . . . Crowley, W. F. (2006). Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes. Molecular and cellular endocrinology, 254, 60-69. https://doi.org/10.1016/j.mce.2006.04.021

Chicago Style (17th ed.) Citation

Pitteloud, Nelly, et al. "Mutations in Fibroblast Growth Factor Receptor 1 Cause Kallmann Syndrome with a Wide Spectrum of Reproductive Phenotypes." Molecular and Cellular Endocrinology 254 (2006): 60-69. https://doi.org/10.1016/j.mce.2006.04.021.

MLA (9th ed.) Citation

Pitteloud, Nelly, 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, 2006, pp. 60-69, https://doi.org/10.1016/j.mce.2006.04.021.