APA (7th ed.) Citation

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.) Citation

Sato, 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.) Citation

Sato, 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.

Warning: These citations may not always be 100% accurate.