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Complex and multi-allelic copy number variation in human disease
Hundreds of copy number variants are complex and multi-allelic, in that they have many structural alleles and have rearranged multiple times in the ancestors who contributed chromosomes to current humans. Not only are the relationships of these multi-allelic CNVs (mCNVs) to phenotypes generally unkn...
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| Publicado no: | Brief Funct Genomics |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4576757/ https://ncbi.nlm.nih.gov/pubmed/26163405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bfgp/elv028 |
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