reference/30935853

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30935853

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	406
issn	0022-2593 1468-6244
issueIdentifier	6
pageRange	396-406
publicationName	Journal of Medical Genetics
startingPage	396
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bibliographicCitation	Kortum F, Das S, Flindt M, Morris-Rosendahl DJ, Stefanova I, Goldstein A, Horn D, Klopocki E, Kluger G, Martin P, Rauch A, Roumer A, Saitta S, Walsh LE, Wieczorek D, Uyanik G, Kutsche K, Dobyns WB. The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. Journal of Medical Genetics. 2011 Mar 25;48(6):396–406. doi: 10.1136/jmg.2010.087528.
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date	2011-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC5522617 https://doi.org/10.1136/jmg.2010.087528 https://pubmed.ncbi.nlm.nih.gov/21441262
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
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