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Human structural variation: mechanisms of chromosome rearrangements

Chromosome structural variation (SV) is a normal part of variation in the human genome, but some classes of SV can cause neurodevelopmental disorders. Analysis of the DNA sequence at SV breakpoints can reveal mutational mechanisms and risk factors for chromosome rearrangement. Large-scale SV breakpo...

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Bibliografski detalji
Izdano u:Trends Genet
Glavni autori: Weckselblatt, Brooke, Rudd, M. Katharine
Format: Artigo
Jezik:Inglês
Izdano: 2015
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4600437/
https://ncbi.nlm.nih.gov/pubmed/26209074
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tig.2015.05.010
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