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Q26858999-1D0F36DF-48A6-4804-826D-15114402DD5B
Q26858999-1D0F36DF-48A6-4804-826D-15114402DD5B
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http://www.wikidata.org/entity/statement/Q26858999-1D0F36DF-48A6-4804-826D-15114402DD5B
A developmental and genetic classification for malformations of cortical development: update 2012
P2860
Q26858999-1D0F36DF-48A6-4804-826D-15114402DD5B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26858999-1D0F36DF-48A6-4804-826D-15114402DD5B
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wasDerivedFrom
a7783db120a307c060612c3af80d4e0f1abe13fa
P2860
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.