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Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome
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  1. Correspondence to:
 Dr M Meins
 Department of Human Genetics, Ruhr-University Bochum, Universitaetsstrasse 150, 44801 Bochum, Germany; moritz.meinsruhr-uni-bochum.de
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Citation

Meins M, Lehmann J, Gerresheim F, et al
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome

Publication history

  • Received June 8, 2004
  • Accepted August 16, 2004
  • Revised August 12, 2004
  • First published February 2, 2005.
Online issue publication 
February 02, 2005

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