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Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
  1. Correspondence to Dr rer. nat. Eva Klopocki, Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany; eva.klopocki{at}charite.de
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Citation

Ott CE, Hein H, Lohan S, et al
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia

Publication history

  • Received March 9, 2012
  • Revised May 17, 2012
  • Accepted May 29, 2012
  • First published June 20, 2012.
Online issue publication 
July 11, 2012

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