The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis (Q33924011)
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English | 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)
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Kerstin Kutsche
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Anita Rauch
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Denise Horn
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Fanny Kortüm
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Soma Das
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Max Flindt
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Deborah J Morris-Rosendahl
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Amy Goldstein
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Gerhard Kluger
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Peter Martin
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Agathe Roumer
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Sulagna Saitta
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Laurence E Walsh
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Dagmar Wieczorek
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Gökhan Uyanik
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