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A large, complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
There is a complex relationship between the evolution of segmental duplications and rearrangements associated with human disease. We performed a detailed analysis of one region on chromosome 16p12.1 associated with neurocognitive disease and identified one of the largest structural inconsistencies w...
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| Główni autorzy: | , , , , , , , , , , , , , , , , |
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| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
2010
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2930074/ https://ncbi.nlm.nih.gov/pubmed/20729854 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.643 |
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