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Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22–q24.1
- Correspondence to: Dr N Wakamatsu Department of Genetics, Institute for Developmental Research, Aichi Human Service Center, 713-8 Kamiya-cho, Kasugai, Aichi 480-0392, Japan; nwakainst-hsc.jp
Citation
Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22–q24.1
Publication history
- Received November 4, 2003
- Accepted January 18, 2004
- First published April 30, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics