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Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel–Giedion syndrome
  1. Correspondence to Dr T Yamamoto, Tokyo Women's Medical University Institute for Integrated Medical Sciences, 8-1 Kawada-cho, Shinjuku-ward, Tokyo 162-8666, Japan; toshiyuki.yamamoto{at}twmu.ac.jp
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Filges I, Shimojima K, Okamoto N, et al
Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel–Giedion syndrome

Publication history

  • Received August 28, 2010
  • Accepted September 13, 2010
  • First published October 30, 2010.
Online issue publication 
January 27, 2011

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