File:Disease Gene Mapping with Multiple Chromosomes.jpg

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English: Description of the general procedure used to identify a disease gene. Regions of the genome (highlighted in red) that could theoretically harbor the disease gene are identified in many affected individuals. Any area where these regions overlap has a high probability of containing the disease gene of interest.
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Author Esherma1

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current05:49, 28 November 2011Thumbnail for version as of 05:49, 28 November 20112,207 × 2,689 (838 KB)Esherma1 (talk | contribs)

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