Martin, K., Norton, M. E., MacPherson, C., Demko, Z., Egbert, M., Haeri, S., Malone, F., Wapner, R. J., Roman, A. S., Khalil, A., Faro, R., Madankumar, R., Strong, N., Silver, R., Vohra, N., Hyett, J., Kao, C., Hakonarson, H., Jacobson, B., & Dar, P. (2023). Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study. Prenatal Diagnosis, 43(13), 1574–1580. Portico. https://doi.org/10.1002/pd.6483