The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis-Reference-Cited by-同舟云学术

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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

Published:2011-03-25 Issue:6 Volume:48 Page:396-406
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Kortum F.,Das S.,Flindt M.,Morris-Rosendahl D. J.,Stefanova I.,Goldstein A.,Horn D.,Klopocki E.,Kluger G.,Martin P.,Rauch A.,Roumer A.,Saitta S.,Walsh L. E.,Wieczorek D.,Uyanik G.,Kutsche K.,Dobyns W. B.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

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