Identifying genetic etiology of CHD
收藏NIAID Data Ecosystem2026-03-13 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP256119
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资源简介：
We aim to identify genetic etiology of CHD using whole genome sequencing and SNP Array. Our findings will rapidly expand our understanding of complex genetics of CHD. SNP Array genotyping data of 11 samples in this ASD pedigree was deposited in GEO database under accession number GSE191116.
创建时间：
2022-04-02
