reference/22152284

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/22152284

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endingPage	922
issn	0969-9961
issueIdentifier	3
pageRange	913-922
publicationName	Neurobiology of Disease
startingPage	913
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bibliographicCitation	Howard ML, Palmer SJ, Taylor KM, Arthurson GJ, Spitzer MW, Du X, Pang TY, Renoir T, Hardeman EC, Hannan AJ. Mutation of Gtf2ird1 from the Williams-Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations. Neurobiol Dis. 2012 Mar;45(3):913–22. doi: 10.1016/j.nbd.2011.12.010. PMID: 22198572.
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date	201203
identifier	https://pubmed.ncbi.nlm.nih.gov/22198572 https://doi.org/10.1016/j.nbd.2011.12.010
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutation of Gtf2ird1 from the Williams–Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations
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