Unal, E. Et Al. 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 , vol.36, no.8 , 739-742.

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 , vol.36, no.8, 739-742.

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, 739-742, 2020

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, pp.739-742, 2020

Unal, E. Et Al. (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 , vol.36, no.8, pp.739-742.

@article{article, author={Edip Unal Et Al. }, title={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}, journal={Gynecological Endocrinology}, year=2020, pages={739-742} }