You are here

  • Home
  • Archive
  • Volume 48, Issue 6
  • The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Citation Tools

Article menu
Download PDFPDF
Phenotypes
Original article
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Download to a citation manager

Download the citation for this article by clicking on one of the following citation managers:

Cite this article as:
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
Journal of Medical Genetics 2011;48:396-406.