Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects

Jeroen Breckpot, B. Thienpont, Y. Arens, L. C. Tranchevent, J.R. Vermeesch, Y. Moreau, M. Gewillig, Koen Devriendt

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)251-259
JournalCytogenetic and Genome Research
Volume135
Issue number3-4
DOIs
Publication statusPublished - 2011

Keywords

  • Algorithm
  • Array CGH
  • Congenital heart defects (CHD)
  • Copy number variation (CNV)
  • Non-syndromic CHD

Cite this

Breckpot, J., Thienpont, B., Arens, Y., Tranchevent, L. C., Vermeesch, J. R., Moreau, Y., Gewillig, M., & Devriendt, K. (2011). Challenges of Interpreting Copy Number Variation in Syndromic and Non-Syndromic Congenital Heart Defects. Cytogenetic and Genome Research, 135(3-4), 251-259. https://doi.org/10.1159/000331272