Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants
Titel:
Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants
Auteur:
Schwab, Marisa E. Dong, Shan Lianoglou, Billie R. Aguilar Lucero, Alessandra F. Schwartz, Grace B. Norton, Mary E. MacKenzie, Tippi C. Sanders, Stephan J.