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- W38604812 abstract "Aim: To visualize copy number associations and quantify relative risk of Copy Number Variants (CNVs) in 100 well-defined congenital heart disease (CHD) risk genes identified from literature sources..." @default.
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- W38604812 date "2011-11-22" @default.
- W38604812 modified "2023-09-26" @default.
- W38604812 title "Abstract 16717: Human Gene Copy Number Spectra Analysis in Congenital Heart Malformations" @default.
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