Associated Papers
Functional FOXC1 variants in familial and sporadic atrial septal defect with cellular and animal validation.
Chen HX et al.
Clinical and Translational Medicine, 2024
Feeding difficulty is the dominant feature in 12 Chinese newborns with CHD7 pathogenic variants.
Chen X et al.
Bmc Medical Genetics, 2019
31146700 (PubMed )
Supplement: 12881_2019_813_MOESM1_ESM.xls › CHD7_ChenXiang_query_Report_Fil
Select a paper to view details