APA (7th ed.) Citation

LP, M., C, K., JM, E., R, W., A, T., SS, B., . . . D, G. (2022). Personalised virtual gene panels reduce interpretation workload and maintain diagnostic rates of proband-only clinical exome sequencing for rare disorders. Journal of medical genetics, 59(4), 393. https://doi.org/10.1136/jmedgenet-2020-107303

Chicago Style (17th ed.) Citation

LP, Molina-Ramírez, et al. "Personalised Virtual Gene Panels Reduce Interpretation Workload and Maintain Diagnostic Rates of Proband-only Clinical Exome Sequencing for Rare Disorders." Journal of Medical Genetics 59, no. 4 (2022): 393. https://doi.org/10.1136/jmedgenet-2020-107303.

MLA (9th ed.) Citation

LP, Molina-Ramírez, et al. "Personalised Virtual Gene Panels Reduce Interpretation Workload and Maintain Diagnostic Rates of Proband-only Clinical Exome Sequencing for Rare Disorders." Journal of Medical Genetics, vol. 59, no. 4, 2022, p. 393, https://doi.org/10.1136/jmedgenet-2020-107303.