APA (7th ed.) Citation

E, B., M, W., A, J., G, K., T, K., K, K., . . . A, G. (2026). Refining the diagnosis of 46,XY disorders of sex development: Insight from whole-exome sequencing. Orphanet journal of rare diseases, 21(1), . https://doi.org/10.1186/s13023-026-04453-9

Chicago Style (17th ed.) Citation

E, Błaszczyk, et al. "Refining the Diagnosis of 46,XY Disorders of Sex Development: Insight from Whole-exome Sequencing." Orphanet Journal of Rare Diseases 21, no. 1 (2026). https://doi.org/10.1186/s13023-026-04453-9.

MLA (9th ed.) Citation

E, Błaszczyk, et al. "Refining the Diagnosis of 46,XY Disorders of Sex Development: Insight from Whole-exome Sequencing." Orphanet Journal of Rare Diseases, vol. 21, no. 1, 2026, https://doi.org/10.1186/s13023-026-04453-9.