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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
scientific article
Author/s
author: William B. Dobyns, Irina Stefanova, Eva Klopocki, Kerstin Kutsche, Anita Rauch, Denise Horn
Work details
Publication date
March 25, 2011
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Language
English
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