APA (7th ed.) Citation

Liu, L., Sun, L., Chen, Y., Wang, M., Yu, C., Huang, Y., . . . group, D. D. I. S. a. C. s. (2022). Delineation of dual molecular diagnosis in patients with skeletal deformity. Orphanet Journal of Rare Diseases, 17(1), 1. https://doi.org/10.1186/s13023-022-02293-x

Chicago Style (17th ed.) Citation

Liu, Lian, et al. "Delineation of Dual Molecular Diagnosis in Patients with Skeletal Deformity." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 1. https://doi.org/10.1186/s13023-022-02293-x.

MLA (9th ed.) Citation

Liu, Lian, et al. "Delineation of Dual Molecular Diagnosis in Patients with Skeletal Deformity." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 1, https://doi.org/10.1186/s13023-022-02293-x.