APA引用形式

Chen, W., Xu, Z., Nishitani, M., Van Ryzin, C., McDonnell, N. B., & Merke, D. P. (2012). Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency.

シカゴスタイル引用形

Chen, Wuyan, Zhi Xu, Miki Nishitani, Carol Van Ryzin, Nazli B. McDonnell, , Deborah P. Merke. Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. 2012.

MLA引用形式

Chen, Wuyan, et al. Complement Component 4 Copy Number Variation and CYP21A2 Genotype Associations in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency. 2012.