APA (7th ed.) Citation

N, S., D, H., W, T., S, S., R, V. C., PJ, C., . . . B, P. (2022). Shortcutting the diagnostic odyssey: The multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA). Orphanet journal of rare diseases, 17(1), 210. https://doi.org/10.1186/s13023-022-02365-y

Chicago Style (17th ed.) Citation

N, Schuermans, et al. "Shortcutting the Diagnostic Odyssey: The Multidisciplinary Program for Undiagnosed Rare Diseases in Adults (UD-PrOZA)." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 210. https://doi.org/10.1186/s13023-022-02365-y.

MLA (9th ed.) Citation

N, Schuermans, et al. "Shortcutting the Diagnostic Odyssey: The Multidisciplinary Program for Undiagnosed Rare Diseases in Adults (UD-PrOZA)." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 210, https://doi.org/10.1186/s13023-022-02365-y.