ロード中...
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have been predicted to play an important role in genetic susceptibility to common disease. To address this we undertook a large direct genome-wide study of association between CNVs and eight common human dis...
保存先:
| フォーマット: | Artigo |
|---|---|
| 言語: | Inglês |
| 出版事項: |
2010
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2892339/ https://ncbi.nlm.nih.gov/pubmed/20360734 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nature08979 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|