Article info
Online mutation report
A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma
- Correspondence to: L A Aaltonen Department of Medical Genetics, Biomedicum Helsinki, P.O. Box 63, FIN-00014 University of Helsinki, Finland; lauri.aaltonenhelsinki.fi
Citation
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
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2005 Journal of Medical Genetics