Article info
Phenotypes
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).
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© 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.