Identifying genetic etiology of CHD using SNP Array. Identifying genetic etiology of CHD using SNP Array
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA789824
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资源简介：
High density genotyping of 7 affected and 3 unaffected family members was performed using the Illumina Omni2.5-8 v1.3 BeadChip SNP. Overall design: To investigate the genetic etiology of the ASD in this multigenerational family, we conducted genome wide linkage analysis on the proband, and also 7 affected and 3 unaffected family members.This analysis yielded three regions with the maximum peak log-of-odds (LOD) score.
创建时间：
2021-12-17
