Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population

@article{An2015GenomewideCN,
  title={Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population},
  author={Y. An and Wen-yuan Duan and G. Huang and Xiaoli Chen and L. Li and Chenxia Nie and Jia Hou and Y. Gui and Yiming Wu and F. Zhang and Y. Shen and Bai-lin Wu and Hongyan Wang},
  journal={BMC Medical Genomics},
  year={2015},
  volume={9}
}
BackgroundVentricular septal defects (VSDs) constitute the most prevalent congenital heart disease (CHD), occurs either in isolation (isolated VSD) or in combination with other cardiac defects (complex VSD). Copy number variation (CNV) has been highlighted as a possible contributing factor to the etiology of many congenital diseases. However, little is known concerning the involvement of CNVs in either isolated or complex VSDs.MethodsWe analyzed 154 unrelated Chinese individuals with VSD by… Expand
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