Genome structural variation and sporadic disease traits

被引:51
作者
Lupski, James R. [1 ]
机构
[1] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Houston, TX 77030 USA
关键词
D O I
10.1038/ng0906-974
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Many submicroscopic genomic rearrangements have been robustly associated with well-defined clinical syndromes. Three papers in this issue once again illustrate how underlying genomic architecture can catalyze rearrangement causing sporadic disease, and they further suggest that widespread clinical implementation of high-resolution genome analysis may identify the cause of traits previously intractable to conventional genetic analyses.
引用
收藏
页码:974 / 976
页数:4
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