The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis (Q33924011)

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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
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    The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis (English)
    Fanny Kortüm
    Deborah J Morris-Rosendahl
    Amy Goldstein
    Gerhard Kluger
    Peter Martin
    Agathe Roumer
    Sulagna Saitta
    Laurence E Walsh
    Dagmar Wieczorek
    Gökhan Uyanik

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