APA (7th ed.) Citation

N, P., Jr, A. J., AU, M., AA, D., FJ, H., & Jr, C. W. (2005). Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene. The Journal of clinical endocrinology and metabolism, 90(3), 1317. https://doi.org/10.1210/jc.2004-1361

Chicago Style (17th ed.) Citation

N, Pitteloud, Acierno JS Jr, Meysing AU, Dwyer AA, Hayes FJ, and Crowley WF Jr. "Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 Gene." The Journal of Clinical Endocrinology and Metabolism 90, no. 3 (2005): 1317. https://doi.org/10.1210/jc.2004-1361.

MLA (9th ed.) Citation

N, Pitteloud, et al. "Reversible Kallmann Syndrome, Delayed Puberty, and Isolated Anosmia Occurring in a Single Family with a Mutation in the Fibroblast Growth Factor Receptor 1 Gene." The Journal of Clinical Endocrinology and Metabolism, vol. 90, no. 3, 2005, p. 1317, https://doi.org/10.1210/jc.2004-1361.