Fanny Kortüm

1. The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
   2011/03/25 by Fanny Kortüm, Soma Das, M. Flindt +22 · 28 citations
   Biochemistry, Genetics and Molecular Biology · #Genetics and Neurodevelopmental Disorders #Genomic variations and chromosomal abnormalities #Genomics and Rare Diseases