Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants
| Autor: | Schwab, Marisa E., Dong, Shan, Lianoglou, Billie R., Aguilar Lucero, Alessandra F., Schwartz, Grace B., Norton, Mary E., MacKenzie, Tippi C., Sanders, Stephan J. |
|---|---|
| Zdroj: | In The American Journal of Surgery January 2022 223(1):182-186 |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|
Full Text from ScienceDirect