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Complex human chromosomal and genomic rearrangements
Copy number variation (CNV) is a major source of genetic variation among humans. In addition to existing as benign polymorphisms, CNVs can also convey clinical phenotypes, including genomic disorders, sporadic diseases and complex human traits. CNV results from genomic rearrangements that can repres...
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| Publié dans: | Trends Genet |
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| Auteurs principaux: | , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2009
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4464790/ https://ncbi.nlm.nih.gov/pubmed/19560228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tig.2009.05.005 |
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