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
Discovery of novel candidate genes for congenital diaphragmatic hernia via whole exome sequencing.
Somayyeh Heidargholizadeh G et al.
Pediatrics International : Official Journal of the Japan Pediatric Society, 0
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