APA (7th ed.) Citation

Mengen, E., Yavaş, A. K., & Uçaktürk, S. A. (2020). A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene. Journal of Clinical Research in Pediatric Endocrinology, 12(2), 206. https://doi.org/10.4274/jcrpe.galenos.2019.2019.0053

Chicago Style (17th ed.) Citation

Mengen, Eda, Aynur Küçükçongar Yavaş, and S. Ahmet Uçaktürk. "A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene." Journal of Clinical Research in Pediatric Endocrinology 12, no. 2 (2020): 206. https://doi.org/10.4274/jcrpe.galenos.2019.2019.0053.

MLA (9th ed.) Citation

Mengen, Eda, et al. "A Rare Etiology of 46,XY Disorder of Sex Development and Adrenal Insufficiency: A Case of MIRAGE Syndrome Caused by Mutations in the SAMD9 Gene." Journal of Clinical Research in Pediatric Endocrinology, vol. 12, no. 2, 2020, p. 206, https://doi.org/10.4274/jcrpe.galenos.2019.2019.0053.