Article info
PDFPhenotypes
Original article
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
- Correspondence to Kerstin Kutsche, Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Campus Forschung, Martinistraße 52, 20246 Hamburg, Germany; kkutsche{at}uke.de and William B Dobyns, Seattle Children's Research Institute Center for Integrative Brain Research, 1900 Ninth Avenue, M/S C9S-10, Seattle WA 98101, USA; wbd{at}uw.edu
Citation
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Publication history
- Received January 5, 2011
- Revised February 7, 2011
- Accepted February 17, 2011
- First published March 25, 2011.
Online issue publication
May 25, 2011
Article Versions
- Previous version (25 March 2011).
- You are viewing the most recent version of this article.
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
© 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.