APA (7th ed.) Citation

Li, Q., Wu, Y., Meng, F., Li, Z., Zhan, D., & Luo, X. (2024). A novel homozygous intronic variant in CDT1 that alters splicing causes Meier–Gorlin syndrome, and a review of published mutations and growth hormone treatments. Orphanet Journal of Rare Diseases, 19(1), 1. https://doi.org/10.1186/s13023-024-03430-4

Chicago Style (17th ed.) Citation

Li, Qing, Yichi Wu, Fucheng Meng, Zhuxi Li, Di Zhan, and Xiaoping Luo. "A Novel Homozygous Intronic Variant in CDT1 That Alters Splicing Causes Meier–Gorlin Syndrome, and a Review of Published Mutations and Growth Hormone Treatments." Orphanet Journal of Rare Diseases 19, no. 1 (2024): 1. https://doi.org/10.1186/s13023-024-03430-4.

MLA (9th ed.) Citation

Li, Qing, et al. "A Novel Homozygous Intronic Variant in CDT1 That Alters Splicing Causes Meier–Gorlin Syndrome, and a Review of Published Mutations and Growth Hormone Treatments." Orphanet Journal of Rare Diseases, vol. 19, no. 1, 2024, p. 1, https://doi.org/10.1186/s13023-024-03430-4.