APA (7th ed.) Citation

G, A., SS, B., AM, B., ML, B., K, B., C, d. L. C., . . . MC, Z. (2023). The International X-Linked Hypophosphatemia (XLH) Registry: First interim analysis of baseline demographic, genetic and clinical data. Orphanet journal of rare diseases, 18(1), 304. https://doi.org/10.1186/s13023-023-02882-4

Chicago Style (17th ed.) Citation

G, Ariceta, et al. "The International X-Linked Hypophosphatemia (XLH) Registry: First Interim Analysis of Baseline Demographic, Genetic and Clinical Data." Orphanet Journal of Rare Diseases 18, no. 1 (2023): 304. https://doi.org/10.1186/s13023-023-02882-4.

MLA (9th ed.) Citation

G, Ariceta, et al. "The International X-Linked Hypophosphatemia (XLH) Registry: First Interim Analysis of Baseline Demographic, Genetic and Clinical Data." Orphanet Journal of Rare Diseases, vol. 18, no. 1, 2023, p. 304, https://doi.org/10.1186/s13023-023-02882-4.