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

التفاصيل البيبلوغرافية
العنوان:	The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
المؤلفون:	Das, Soma, Flindt, Max, Morris-Rosendahl, Deborah J., Stefanova, Irina, Goldstein, Amy, Horn, Denise, Klopocki, Eva, Kluger, Gerhard, Martin, Peter, Rauch, Anita, Roumer, Agathe, Saitta, Sulagna, Walsh, Laurence E., Wieczorek, Dagmar, Uyanik, Gökhan, Kutsche, Kerstin, Dobyns, William B., Kortüm, Fanny
الوصول الحر:	https://www.europeana.eu/item/2048441/item_DCTG65K4HSBNNFSQCQAARTFDECEN3U3C?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCaTest
قاعدة البيانات:	Europeana

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