Cite
Idiopathic hypogonadotropic hypogonadism caused by compound heterozygosity for two novel mutations in the GNRH1 gene: a case report.
MLA
Tian, Qingqing, et al. “Idiopathic Hypogonadotropic Hypogonadism Caused by Compound Heterozygosity for Two Novel Mutations in the GNRH1 Gene: A Case Report.” BMC Endocrine Disorders, vol. 23, no. 1, Oct. 2023, pp. 1–7. EBSCOhost, https://doi.org/10.1186/s12902-023-01455-7.
APA
Tian, Q., Tang, J., Wang, L., Liu, J., Li, X., Cao, Z., & Tian, Z. (2023). Idiopathic hypogonadotropic hypogonadism caused by compound heterozygosity for two novel mutations in the GNRH1 gene: a case report. BMC Endocrine Disorders, 23(1), 1–7. https://doi.org/10.1186/s12902-023-01455-7
Chicago
Tian, Qingqing, Jingjing Tang, Lihong Wang, Jiaojiao Liu, Xiangshan Li, Zhuozhuo Cao, and Zhufang Tian. 2023. “Idiopathic Hypogonadotropic Hypogonadism Caused by Compound Heterozygosity for Two Novel Mutations in the GNRH1 Gene: A Case Report.” BMC Endocrine Disorders 23 (1): 1–7. doi:10.1186/s12902-023-01455-7.