Freud, L. R., Galloway, S., Crowley, T. B., Moldenhauer, J., Swillen, A., Breckpot, J., Borrell, A., Vora, N. L., Cuneo, B., Hoffman, H., Gilbert, L., Nowakowska, B., Geremek, M., Kutkowska-Kaźmierczak, A., Vermeesch, J. R., Devriendt, K., Busa, T., Sigaudy, S., Vigneswaran, T., … McDonald-McGinn, D. M. (2024). Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age. American Journal of Obstetrics and Gynecology, 230(3), 368.e1-368.e12. https://doi.org/10.1016/j.ajog.2023.09.005

Meadows, J. J., Bauser-Heaton, H., Petit, C. J., Goldstein, B. H., Qureshi, A. M., McCracken, C. E., Kelleman, M. S., Nicholson, G. T., Law, M. A., Zampi, J. D., Shahanavaz, S., Chai, P. J., Romano, J. C., Batlivala, S. P., Maskatia, S. A., Asztalos, I. B., Eilers, L., Kamsheh, A. M., Healan, S. J., … Mascio, C. E. (2023). Comparison of treatment strategies for neonates with tetralogy of Fallot and pulmonary atresia. The Journal of Thoracic and Cardiovascular Surgery, 166(3), 916-925.e6. https://doi.org/10.1016/j.jtcvs.2023.01.008

Mustillo, P. J., Sullivan, K. E., Chinn, I. K., Notarangelo, L. D., Haddad, E., Davies, E. G., de la Morena, M. T., Hartog, N., Yu, J. E., Hernandez-Trujillo, V. P., Ip, W., Franco, J., Gambineri, E., Hickey, S. E., Varga, E., & Markert, M. L. (2023). Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development. Journal of Clinical Immunology, 43(2), 247–270. https://doi.org/10.1007/s10875-022-01418-y

Dar, P., Jacobsson, B., Clifton, R., Egbert, M., Malone, F., Wapner, R. J., Roman, A. S., Khalil, A., Faro, R., Madankumar, R., Edwards, L., Strong, N., Haeri, S., Silver, R., Vohra, N., Hyett, J., Demko, Z., Martin, K., Rabinowitz, M., … Norton, M. E. (2022). Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome. American Journal of Obstetrics and Gynecology, 227(1), 79.e1-79.e11. https://doi.org/10.1016/j.ajog.2022.01.002