APA (7th ed.) Citation

JR, L., D, M., D, L., T, N., TB, C., OT, T., . . . BE, M. (2026). Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome. MedRxiv : the preprint server for health sciences. https://doi.org/10.64898/2026.02.23.26346918

Chicago Style (17th ed.) Citation

JR, Lin, et al. "Deletion Size and Background Genetic Variation Shape Congenital Heart Disease Phenotypes in 3,016 Individuals with 22q11.2 Deletion Syndrome." MedRxiv : The Preprint Server for Health Sciences 2026. https://doi.org/10.64898/2026.02.23.26346918.

MLA (9th ed.) Citation

JR, Lin, et al. "Deletion Size and Background Genetic Variation Shape Congenital Heart Disease Phenotypes in 3,016 Individuals with 22q11.2 Deletion Syndrome." MedRxiv : The Preprint Server for Health Sciences, 2026, https://doi.org/10.64898/2026.02.23.26346918.