The PREGCARE study: Personalized recurrence risk assessment following the birth of a child with a pathogenic de novo mutation

Bernkopf M., Abdullah U., Bush S., Wood K., Ghaffari S., Giannoulatou E., Koelling N., Maher G., Thibault L., Williams J., Blair E., Kelly FB., Bloss A., Burkitt-Wright E., Canham N., Deng A., Dixit A., Eason J., Elmslie F., Gardham A., Hay E., Holder M., Homfray T., Hurst J., Johnson D., Jones W., Kini U., Kivuva E., Kumar A., Lees M., Leitch H., Morton J., Németh A., Ramachandrappa S., Saunders K., Shears D., Side L., Splitt M., Stewart A., Stewart H., Suri M., Clouston P., Davies R., Wilkie A., Goriely A.

DOI

10.1101/2022.07.26.501520

Type

Preprint

Publication Date

2022

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