DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Kortüm F, Das S, Flindt M , et al.
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
J Med Genet 2011;
48 (6) 396-406
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