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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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| Vydáno v: | Brief Funct Genomics |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2015
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| Témata: | |
| On-line přístup: | 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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