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Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment

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dc.contributor.authorCeroni, Fabiola
dc.contributor.authorSimpson, Nuala H
dc.contributor.authorFrancks, Clyde
dc.contributor.authorBaird, Gillian
dc.contributor.authorConti-Ramsden, Gina
dc.contributor.authorClark, Ann
dc.contributor.authorBolton, Patrick F
dc.contributor.authorHennessy, Elizabeth R
dc.contributor.authorDonnelly, Peter
dc.contributor.authorBentley, David R
dc.contributor.authorMartin, Hilary
dc.contributor.authorParr, Jeremy
dc.contributor.authorPagnamenta, Alistair T
dc.contributor.authorMaestrini, Elena
dc.contributor.authorBacchelli, Elena
dc.contributor.authorFisher, Simon E
dc.contributor.authorNewbury, Dianne F
dc.contributor.authorIMGSAC
dc.contributor.institutionUniversity of Aberdeen.Medical Educationen
dc.date.accessioned2015-01-27T11:20:01Z
dc.date.available2015-01-27T11:20:01Z
dc.date.issued2014-10
dc.description.statusPeer revieweden
dc.format.extent7
dc.format.extent1519222
dc.identifier45921985
dc.identifier74da4b77-925b-410c-9116-1f60dc742031
dc.identifier24518835
dc.identifier84898664030
dc.identifier.citationCeroni, F, Simpson, N H, Francks, C, Baird, G, Conti-Ramsden, G, Clark, A, Bolton, P F, Hennessy, E R, Donnelly, P, Bentley, D R, Martin, H, Parr, J, Pagnamenta, A T, Maestrini, E, Bacchelli, E, Fisher, S E, Newbury, D F & IMGSAC 2014, 'Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment', EJHG : European journal of human genetics : the official journal of the European Society of Human Genetics. , vol. 22, no. 10, pp. 1165-1171. https://doi.org/10.1038/ejhg.2014.4en
dc.identifier.doi10.1038/ejhg.2014.4
dc.identifier.iss10en
dc.identifier.issn1018-4813
dc.identifier.urihttp://hdl.handle.net/2164/4209
dc.identifier.vol22en
dc.language.isoeng
dc.relation.ispartofEJHG : European journal of human genetics : the official journal of the European Society of Human Genetics.en
dc.subjectZNF277en
dc.subjectSLIen
dc.subjectlanguageen
dc.subjectR Medicineen
dc.subject.lccRen
dc.titleHomozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairmenten
dc.typeJournal articleen

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