APA (7th ed.) Citation

Liu, H., Ran, J., Chen, C., Chen, G., Zhu, P., Tan, R., & Liu, Y. A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia. Wiley.

Chicago Style (17th ed.) Citation

Liu, Hongbing, Jianmin Ran, Chuping Chen, Guangshu Chen, Ping Zhu, Rongshao Tan, and Yan Liu. A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) Due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia. Wiley.

MLA (9th ed.) Citation

Liu, Hongbing, et al. A Chinese Family with Familial Dysalbuminemic Hyperthyroxinemia (FDH) Due to R242H Mutation on Human Albumin Gene: Reevaluating the Role of FDH in Patients with Asymptomatic Hyperthyroxinemia. Wiley.