Associated Papers
Genetic findings of children with congenital heart diseases using chromosomal microarray and trio-based whole exome sequencing.
Guo R et al.
Scientific Reports, 2025
40715143 (PubMed )
Supplement: 41598_2025_6977_MOESM2_ESM.xlsx › Sheet1
Identification of a novel mutation in a Chinese family with Nance-Horan syndrome by whole exome sequencing.
Hong N et al.
Journal of Zhejiang University. Science. B, 2014
Select a paper to view details