A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene.

MLA

Unal, Edip, et al. “A Rare Cause of Delayed Puberty in Two Cases with 46,XX and 46,XY Karyotype: 17 α-Hydroxylase Deficiency Due to a Novel Variant in CYP17A1 Gene.” Gynecological Endocrinology, vol. 36, no. 8, Aug. 2020, pp. 739–42. EBSCOhost, https://doi.org/10.1080/09513590.2019.1707798.

APA

Unal, E., Yıldırım, R., Taş, F. F., Tekin, S., Ceylaner, S., & Haspolat, Y. K. (2020). A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene. Gynecological Endocrinology, 36(8), 739–742. https://doi.org/10.1080/09513590.2019.1707798

Chicago

Unal, Edip, Ruken Yıldırım, Funda Feryal Taş, Suat Tekin, Serdar Ceylaner, and Yusuf Kenan Haspolat. 2020. “A Rare Cause of Delayed Puberty in Two Cases with 46,XX and 46,XY Karyotype: 17 α-Hydroxylase Deficiency Due to a Novel Variant in CYP17A1 Gene.” Gynecological Endocrinology 36 (8): 739–42. doi:10.1080/09513590.2019.1707798.