Associated Papers
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.
Ganapathi M et al.
European Journal of Human Genetics : Ejhg, 2023
De novo frameshift mutation in COUP-TFII (NR2F2) in human congenital diaphragmatic hernia.
High FA et al.
American Journal of Medical Genetics. Part A, 2016
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