APA (7th ed.) Citation

V, N., P, F., M, T., GA, T., M, S., F, C., . . . LA, P. (2020). GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature. Frontiers in endocrinology, 11, 626. https://doi.org/10.3389/fendo.2020.00626

Chicago Style (17th ed.) Citation

V, Neocleous, et al. "GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature." Frontiers in Endocrinology 11 (2020): 626. https://doi.org/10.3389/fendo.2020.00626.

MLA (9th ed.) Citation

V, Neocleous, et al. "GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of the Literature." Frontiers in Endocrinology, vol. 11, 2020, p. 626, https://doi.org/10.3389/fendo.2020.00626.