reference/31739032

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/31739032

Outgoing Links

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endingPage	339
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pageRange	336-339
publicationName	European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
startingPage	336
bibliographicCitation	Caporali C, Signorini S, De Giorgis V, Pichiecchio A, Zuffardi O, Orcesi S. Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1 -related syndrome. European Journal of Paediatric Neurology. 2018 Mar;22(2):336–9. doi: 10.1016/j.ejpn.2018.01.007.
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date	201803
identifier	https://doi.org/10.1016/j.ejpn.2018.01.007 https://pubmed.ncbi.nlm.nih.gov/29396177
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1 -related syndrome
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Total number of triples: 46.