D. Kaya Et Al. , "CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report.," 15. Ulusal Tıbbi Genetik Kongresi , Muğla, Turkey, pp.226, 2022
Kaya, D. Et Al. 2022. CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report.. 15. Ulusal Tıbbi Genetik Kongresi , (Muğla, Turkey), 226.
Kaya, D., Tekin, K., Karakılıç, E., & Sılan, F., (2022). CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report. . 15. Ulusal Tıbbi Genetik Kongresi (pp.226). Muğla, Turkey
Kaya, Derya Et Al. "CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report.," 15. Ulusal Tıbbi Genetik Kongresi, Muğla, Turkey, 2022
Kaya, Derya Et Al. "CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report.." 15. Ulusal Tıbbi Genetik Kongresi , Muğla, Turkey, pp.226, 2022
Kaya, D. Et Al. (2022) . "CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report.." 15. Ulusal Tıbbi Genetik Kongresi , Muğla, Turkey, p.226.
@conferencepaper{conferencepaper, author={Derya Kaya Et Al. }, title={CYP11B1 homozygous mutation in congenital adrenal hyperplasia: A case report.}, congress name={15. Ulusal Tıbbi Genetik Kongresi}, city={Muğla}, country={Turkey}, year={2022}, pages={226} }