Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA).

MLA

Schuermans, Nika, 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, May 2022, p. 210. EBSCOhost, https://doi.org/10.1186/s13023-022-02365-y.

APA

Schuermans, N., Hemelsoet, D., Terryn, W., Steyaert, S., Van Coster, R., Coucke, P. J., Steyaert, W., Callewaert, B., Bogaert, E., Verloo, P., Vanlander, A. V., Debackere, E., Ghijsels, J., LeBlanc, P., Verdin, H., Naesens, L., Haerynck, F., Callens, S., Dermaut, B., & Poppe, B. (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

Schuermans, Nika, Dimitri Hemelsoet, Wim Terryn, Sanne Steyaert, Rudy Van Coster, Paul J Coucke, Wouter Steyaert, et al. 2022. “Shortcutting the Diagnostic Odyssey: The Multidisciplinary Program for Undiagnosed Rare Diseases in Adults (UD-PrOZA).” Orphanet Journal of Rare Diseases 17 (1): 210. doi:10.1186/s13023-022-02365-y.