APA (7th ed.) Citation

Li, S., Hua, R., Han, X., Xu, Y., Li, M., Gao, L., . . . Wang, Y. (2025). Targeted long-read sequencing facilitates effective carrier screening for complex monogenic diseases including spinal muscular atrophy, α-/β-thalassemia, 21-hydroxylase deficiency, and fragile-X syndrome. Journal of Translational Medicine, 23(1), 1. https://doi.org/10.1186/s12967-025-06345-1

Chicago Style (17th ed.) Citation

Li, Shuyuan, et al. "Targeted Long-read Sequencing Facilitates Effective Carrier Screening for Complex Monogenic Diseases Including Spinal Muscular Atrophy, α-/β-thalassemia, 21-hydroxylase Deficiency, and Fragile-X Syndrome." Journal of Translational Medicine 23, no. 1 (2025): 1. https://doi.org/10.1186/s12967-025-06345-1.

MLA (9th ed.) Citation

Li, Shuyuan, et al. "Targeted Long-read Sequencing Facilitates Effective Carrier Screening for Complex Monogenic Diseases Including Spinal Muscular Atrophy, α-/β-thalassemia, 21-hydroxylase Deficiency, and Fragile-X Syndrome." Journal of Translational Medicine, vol. 23, no. 1, 2025, p. 1, https://doi.org/10.1186/s12967-025-06345-1.