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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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| Publicado no: | Trends Genet |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | 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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