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(ORCID: 0000-0003-2930-3163)
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Artikel
Kortüm, Fanny, Das, Soma, Flindt, Max, Uyanik, Gökhan 
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(2011)
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis.
Journal of Medical Genetics 48, S. 396-406.
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