Associated Papers
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia.
Pendleton KE et al.
Journal of Pediatric Genetics, 2024
De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.
Qi H et al.
Plos Genetics, 2018
30532227 (PubMed )
Supplement: pgen.1007822.s011.xlsx › CodingDNM
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