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A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma
  1. Correspondence to:
 L A Aaltonen
 Department of Medical Genetics, Biomedicum Helsinki, P.O. Box 63, FIN-00014 University of Helsinki, Finland; lauri.aaltonenhelsinki.fi
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Citation

Hienonen T, Sammalkorpi H, Isohanni P, et al
A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma

Publication history

  • Received May 18, 2004
  • Accepted September 2, 2004
  • Revised August 6, 2004
  • First published January 5, 2005.
Online issue publication 
April 27, 2016

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