The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Fanny Kortüm, Soma Das, Max Flindt, Deborah J. Morris-Rosendahl, Irina Stefanova, Amy Goldstein, Denise Horn, Eva Klopocki, Gerhard Kluger, Peter Martin, Anita Rauch, Agathe Roumer, Sulagna Saitta, Laurence E. Walsh, Dagmar Wieczorek, Gökhan Uyanik, Kerstin Kutsche*, William B. Dobyns

*Corresponding author for this work
101 Citations (Scopus)

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Medicine & Life Sciences