APA (7th ed.) Citation

Pagnamenta, A. T., Camps, C., Giacopuzzi, E., Taylor, J. M., Hashim, M., Calpena, E., . . . Taylor, J. C. (2023). Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases. Genome Medicine, 15(1), . https://doi.org/10.1186/s13073-023-01240-0

Chicago Style (17th ed.) Citation

Pagnamenta, Alistair T., et al. "Structural and Non-coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases." Genome Medicine 15, no. 1 (2023). https://doi.org/10.1186/s13073-023-01240-0.

MLA (9th ed.) Citation

Pagnamenta, Alistair T., et al. "Structural and Non-coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases." Genome Medicine, vol. 15, no. 1, 2023, https://doi.org/10.1186/s13073-023-01240-0.