Cite
Congenital hypogonadotropic hypogonadism in a patient with a de novo POGZ mutation.
MLA
Eskici, Nazli, et al. “Congenital Hypogonadotropic Hypogonadism in a Patient with a de Novo POGZ Mutation.” European Journal of Endocrinology, vol. 189, no. 2, Aug. 2023, pp. 271–80. EBSCOhost, https://doi.org/10.1093/ejendo/lvad111.
APA
Eskici, N., Madhusudan, S., Vaaralahti, K., Yellapragada, V., Gomez-Sanchez, C., Kärkinen, J., Almusa, H., Brandstack, N., Miettinen, P. J., Wang, Y., & Raivio, T. (2023). Congenital hypogonadotropic hypogonadism in a patient with a de novo POGZ mutation. European Journal of Endocrinology, 189(2), 271–280. https://doi.org/10.1093/ejendo/lvad111
Chicago
Eskici, Nazli, Shrinidhi Madhusudan, Kirsi Vaaralahti, Venkatram Yellapragada, Celia Gomez-Sanchez, Juho Kärkinen, Henrikki Almusa, et al. 2023. “Congenital Hypogonadotropic Hypogonadism in a Patient with a de Novo POGZ Mutation.” European Journal of Endocrinology 189 (2): 271–80. doi:10.1093/ejendo/lvad111.