| Literature DB >> 10866211 |
Abstract
Human genetics is now at a critical juncture. The molecular methods used successfully to identify the genes underlying rare mendelian syndromes are failing to find the numerous genes causing more common, familial, non-mendelian diseases. With the human genome sequence nearing completion, new opportunities are being presented for unravelling the complex genetic basis of non-mendelian disorders based on large-scale genome-wide studies. Considerable debate has arisen regarding the best approach to take. In this review I discuss these issues, together with suggestions for optimal post-genome strategies.Entities:
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Year: 2000 PMID: 10866211 DOI: 10.1038/35015718
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962