APA (7th ed.) Citation

C, S., L, E. K., PA, R., N, C., M, B., N, R., . . . D, S. (2025). Resolving structural variations missed by short-read sequencing uncovers their pathogenicity. Journal of medical genetics, 62(12), 750. https://doi.org/10.1136/jmg-2025-110838

Chicago Style (17th ed.) Citation

C, Schluth-Bolard, et al. "Resolving Structural Variations Missed by Short-read Sequencing Uncovers Their Pathogenicity." Journal of Medical Genetics 62, no. 12 (2025): 750. https://doi.org/10.1136/jmg-2025-110838.

MLA (9th ed.) Citation

C, Schluth-Bolard, et al. "Resolving Structural Variations Missed by Short-read Sequencing Uncovers Their Pathogenicity." Journal of Medical Genetics, vol. 62, no. 12, 2025, p. 750, https://doi.org/10.1136/jmg-2025-110838.