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The core FOXG1 syndrome phenotype consists of postnatal m... | ResearchHub
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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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Authors
Fanny Kortüm
17 more
Fanny Kortüm
•
Soma Das
15 more
•
William Dobyns
Published
March 25, 2011
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Journal
Journal of Medical Genetics
Topics
Biology
Neuroscience
Medicine
Pediatrics
Genetics
Show all topics
DOI
10.1136/jmg.2010.087528
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Journal of Medical Genetics
Topics
Biology
Neuroscience
Medicine
Pediatrics
Genetics
Show all topics
DOI
10.1136/jmg.2010.087528
Other Formats
PDF
