APA (7th ed.) Citation

Akcan, N., Uyguner, O., Baş, F., Altunoğlu, U., Toksoy, G., Karaman, B., . . . Darendeliler, F. (2022). Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD. Journal of Clinical Research in Pediatric Endocrinology, 14(2), 153. https://doi.org/10.4274/jcrpe.galenos.2022.2021-9-19

Chicago Style (17th ed.) Citation

Akcan, Neşe, et al. "Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD." Journal of Clinical Research in Pediatric Endocrinology 14, no. 2 (2022): 153. https://doi.org/10.4274/jcrpe.galenos.2022.2021-9-19.

MLA (9th ed.) Citation

Akcan, Neşe, et al. "Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD." Journal of Clinical Research in Pediatric Endocrinology, vol. 14, no. 2, 2022, p. 153, https://doi.org/10.4274/jcrpe.galenos.2022.2021-9-19.