Editorial
doi: 10.1038/ng0906-959.
Structural variants deconstruct the genome
- PMID: 16940994
- DOI: 10.1038/ng0906-959
Item in Clipboard
Editorial
Structural variants deconstruct the genome
Nat Genet.
2006 Sep.
Abstract
Common genomic structural variants predispose to deleterious de novo genomic rearrangements. Understanding how they do so will require population studies across the continuum of genomic variation and ethical discussion of the nature and uses of human variation.
Comment on
-
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.Nat Genet. 2006 Sep;38(9):1038-42. doi: 10.1038/ng1862. Epub 2006 Aug 13. Nat Genet. 2006. PMID: 16906162
-
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability.Nat Genet. 2006 Sep;38(9):1032-7. doi: 10.1038/ng1858. Epub 2006 Aug 13. Nat Genet. 2006. PMID: 16906163
-
Genome structural variation and sporadic disease traits.Nat Genet. 2006 Sep;38(9):974-6. doi: 10.1038/ng0906-974. Nat Genet. 2006. PMID: 16941003 No abstract available.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
