APA (7th ed.) Citation

N, B., N, K., AG, C., B, C., J, M., & JS, M. (2024). Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2. Prenatal diagnosis, 44(5), 661. https://doi.org/10.1002/pd.6560

Chicago Style (17th ed.) Citation

N, Burrill, Khalek N, Cristancho AG, Coleman B, Murrell J, and Moldenhauer JS. "Fetus with Multiple Congenital Anomaly Syndrome Caused by Novel Variant in ATP1A2." Prenatal Diagnosis 44, no. 5 (2024): 661. https://doi.org/10.1002/pd.6560.

MLA (9th ed.) Citation

N, Burrill, et al. "Fetus with Multiple Congenital Anomaly Syndrome Caused by Novel Variant in ATP1A2." Prenatal Diagnosis, vol. 44, no. 5, 2024, p. 661, https://doi.org/10.1002/pd.6560.

Warning: These citations may not always be 100% accurate.