APA (7th ed.) Citation

A, S., C, M., K, S., A, V., M, R., C, R., . . . BS, S. (2025). Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay. American journal of medical genetics. Part A, 197(10), e64119. https://doi.org/10.1002/ajmg.a.64119

Chicago Style (17th ed.) Citation

A, Strong, et al. "Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay." American Journal of Medical Genetics. Part A 197, no. 10 (2025): e64119. https://doi.org/10.1002/ajmg.a.64119.

MLA (9th ed.) Citation

A, Strong, et al. "Truncating Variants in RREB1 Cause a Novel RASopathy Syndrome of Congenital Heart Disease, Genitourinary Malformations, and Developmental Delay." American Journal of Medical Genetics. Part A, vol. 197, no. 10, 2025, p. e64119, https://doi.org/10.1002/ajmg.a.64119.