APA (7th ed.) Citation

SW, C., JC, C., TH, B., JC, M., SM, W., ML, M., . . . EJ, L. (2023). Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes. Human genetics, 142(10), 1531. https://doi.org/10.1007/s00439-023-02596-4

Chicago Style (17th ed.) Citation

SW, Curtis, et al. "Rare Variant Modifier Analysis Identifies Variants in SEC24D Associated with Orofacial Cleft Subtypes." Human Genetics 142, no. 10 (2023): 1531. https://doi.org/10.1007/s00439-023-02596-4.

MLA (9th ed.) Citation

SW, Curtis, et al. "Rare Variant Modifier Analysis Identifies Variants in SEC24D Associated with Orofacial Cleft Subtypes." Human Genetics, vol. 142, no. 10, 2023, p. 1531, https://doi.org/10.1007/s00439-023-02596-4.