APA (7th ed.) Citation

G, P., ML, F., N, P., J, L., DM, K., KM, C., . . . JL, M. (2022). Exome sequencing identifies variants in infants with sacral agenesis. Birth defects research, 114(7), 215. https://doi.org/10.1002/bdr2.1987

Chicago Style (17th ed.) Citation

G, Pitsava, et al. "Exome Sequencing Identifies Variants in Infants with Sacral Agenesis." Birth Defects Research 114, no. 7 (2022): 215. https://doi.org/10.1002/bdr2.1987.

MLA (9th ed.) Citation

G, Pitsava, et al. "Exome Sequencing Identifies Variants in Infants with Sacral Agenesis." Birth Defects Research, vol. 114, no. 7, 2022, p. 215, https://doi.org/10.1002/bdr2.1987.