Research Letter

Pitfalls in the use of DGV for CNV interpretation†

  1. Aude Duclos1,2,
  2. Françoise Charbonnier1,2,
  3. Pascal Chambon1,2,
  4. Jean-Baptiste Latouche1,2,
  5. André Blavier3,
  6. Richard Redon4,
  7. Thierry Frébourg1,2,*,
  8. Jean-Michel Flaman1

Article first published online: 9 SEP 2011

DOI: 10.1002/ajmg.a.34195

Issue

American Journal of Medical Genetics Part A

American Journal of Medical Genetics Part A

Volume 155, Issue 10, pages 2593–2596, October 2011

Additional Information

How to Cite

Duclos, A., Charbonnier, F., Chambon, P., Latouche, J.-B., Blavier, A., Redon, R., Frébourg, T. and Flaman, J.-M. (2011), Pitfalls in the use of DGV for CNV interpretation. Am. J. Med. Genet., 155: 2593–2596. doi: 10.1002/ajmg.a.34195

Author Information

  1. 1

    Inserm U614, Faculty of Medicine, Rouen University, Rouen, France

  2. 2

    Institute for Medical Research and Innovation, Department of Genetics, University Hospital, Rouen, France

  3. 3

    Interactive Biosoftware, Rouen, France

  4. 4

    Inserm UMR 915, L'institut du thorax, University Hospital, Nantes, France

*Molecular Genetics, Faculty of Medicine, 22 Boulevard Gambetta, 76183 Rouen, France.

  1. †

    How to Cite this Article: Duclos A, Charbonnier F, Chambon P, Latouche J-B, Blavier A, Redon R, Frébourg T, Flaman J-M. 2011. Pitfalls in the use of DGV for CNV interpretation. Am J Med Genet Part A 155:2593–2596.

Publication History

  1. Issue published online: 20 SEP 2011
  2. Article first published online: 9 SEP 2011
  3. Manuscript Accepted: 1 JUN 2011
  4. Manuscript Received: 8 JAN 2011

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