Prenatal Diagnosis

Displaying 1 - 4 of 4CSV
Reilly, K., Sonner, S., McCay, N., Rolnik, D. L., Casey, F., Seale, A. N., Watson, C. J., Kan, A., Lai, T. H. T., Chung, B. H. Y., Diderich, K. E. M., Srebniak, M. I., Dempsey, E., Drury, S., Giordano, J., Wapner, R., Kilby, M. D., Chitty, L. S., & Mone, F. (2024). The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta‐analysis. Prenatal Diagnosis, 44(6–7), 821–831. Portico. https://doi.org/10.1002/pd.6581
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Bellair, M., Amaral, E., Ouren, M., Roark, C., Kim, J., O’Connor, A., Soriano, A., Schindler, M. L., Wapner, R. J., Stone, J. L., Tavella, N., Merriam, A., Perley, L., Breman, A. M., & Beaudet, A. L. (2024). Noninvasive single‐cell‐based prenatal genetic testing: A proof of concept clinical study. Prenatal Diagnosis, 44(3), 304–316. Portico. https://doi.org/10.1002/pd.6529
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Duyzend, M. H., Cacheiro, P., Jacobsen, J. O. B., Giordano, J., Brand, H., Wapner, R. J., Talkowski, M. E., Robinson, P. N., & Smedley, D. (2024). Improving prenatal diagnosis through standards and aggregation. Prenatal Diagnosis, 44(4), 454–464. Portico. https://doi.org/10.1002/pd.6522
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Van den Veyver, I. B., Chandler, N., Wilkins‐Haug, L. E., Wapner, R. J., & Chitty, L. S. (2022). International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis. Prenatal Diagnosis, 42(6), 796–803. Portico. https://doi.org/10.1002/pd.6157
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