Associated Papers
Exome analysis links kidney malformations to developmental disorders and reveals causal genes.
Milo Rasouly H et al.
Nature Communications, 2025
40774958 (PubMed )
Supplement: 41467_2025_62319_MOESM5_ESM.xlsx › D10-Candidate_Genes
Meta-analysis reveals transcription factors and DNA binding domain variants associated with congenital heart defect and orofacial cleft.
Jeong R et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
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
Select a paper to view details