Sato, N., Hasegawa, T., Hori, N., Fukami, M., Yoshimura, Y., & Ogata, T. (2005). Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: Report of three families:Case report. Human reproduction (Oxford), 20(8), 2173-2178. https://doi.org/10.1093/humrep/dei052
Chicago Style (17th ed.) CitationSato, Naoko, Tomonobu Hasegawa, Naoaki Hori, Maki Fukami, Yasunori Yoshimura, and Tsutomu Ogata. "Gonadotrophin Therapy in Kallmann Syndrome Caused by Heterozygous Mutations of the Gene for Fibroblast Growth Factor Receptor 1: Report of Three Families:Case Report." Human Reproduction (Oxford) 20, no. 8 (2005): 2173-2178. https://doi.org/10.1093/humrep/dei052.
MLA (9th ed.) CitationSato, Naoko, et al. "Gonadotrophin Therapy in Kallmann Syndrome Caused by Heterozygous Mutations of the Gene for Fibroblast Growth Factor Receptor 1: Report of Three Families:Case Report." Human Reproduction (Oxford), vol. 20, no. 8, 2005, pp. 2173-2178, https://doi.org/10.1093/humrep/dei052.