Siklar, Z. Et Al. 2024. 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.. Endocrine , vol.85, no.3 , 1407-1416.

Siklar, Z., Camtosun, E., Bolu, S., Yildiz, M., Akinci, A., Bas, F., ... Dündar, İ.(2024). 17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.. Endocrine , vol.85, no.3, 1407-1416.

Siklar, Zeynep Et Al. "17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.," Endocrine , vol.85, no.3, 1407-1416, 2024

Siklar, Zeynep Et Al. "17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.." Endocrine , vol.85, no.3, pp.1407-1416, 2024

Siklar, Z. Et Al. (2024) . "17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.." Endocrine , vol.85, no.3, pp.1407-1416.

@article{article, author={Zeynep Siklar Et Al. }, title={17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort.}, journal={Endocrine}, year=2024, pages={1407-1416} }