Identifying genetic etiology of CHD using SNP Array
Ontology highlight
ABSTRACT: High density genotyping of 7 affected and 3 unaffected family members was performed using the Illumina Omni2.5-8 v1.3 BeadChip SNP.
ORGANISM(S): Homo sapiens
PROVIDER: GSE191116 | GEO | 2021/12/31
REPOSITORIES: GEO
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