Copy-number variation and association studies of human disease
Copy-number variation and association studies of human disease
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Publisher
United States: Nature Publishing Group
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Language
English
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Publisher
United States: Nature Publishing Group
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Contents
The central goal of human genetics is to understand the inherited basis of human variation in phenotypes, elucidating human physiology, evolution and disease. Rare mutations have been found underlying two thousand mendelian diseases; more recently, it has become possible to assess systematically the contribution of common SNPs to complex disease. T...
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Full title
Copy-number variation and association studies of human disease
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TN_cdi_proquest_miscellaneous_877597700
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_877597700
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ISSN
1061-4036
E-ISSN
1546-1718
DOI
10.1038/ng2080
