The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

<div>Illumina HumanOmni1-Quad SNP array indicates a shared region of homozygosity on chromosome 2q31.1. This region is approximately 2.9 Mb and contains<i> DCAF17</i>, the gene associated with WSS. This graphic was constructed using the UCSC Genome Browser (GRCh37/hg19).</div>

Case Reports in Genetics

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Figure 2: The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome 

Figure 2 | The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome 