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dc.contributor.authorNudel, R.
dc.contributor.authorSimpson, N. H.
dc.contributor.authorBaird, G.
dc.contributor.authorO'Hare, A.
dc.contributor.authorConti-Ramsden, G.
dc.contributor.authorBolton, P. F.
dc.contributor.authorHennessy, E. R.
dc.contributor.authorRing, S. M.
dc.contributor.authorSmith, G. Davey
dc.contributor.authorFrancks, C.
dc.contributor.authorParacchini, S.
dc.contributor.authorMonaco, A. P.
dc.contributor.authorFisher, S. E.
dc.contributor.authorNewbury, D. F.
dc.contributor.authorSLI Consortium
dc.date.accessioned2015-02-06T16:37:01Z
dc.date.available2015-02-06T16:37:01Z
dc.date.issued2014-04
dc.identifier45922067
dc.identifier559ea20a-5ae0-4cdc-9d25-618f47c94ee1
dc.identifier000333887500007
dc.identifier84897958382
dc.identifier.citationNudel , R , Simpson , N H , Baird , G , O'Hare , A , Conti-Ramsden , G , Bolton , P F , Hennessy , E R , Ring , S M , Smith , G D , Francks , C , Paracchini , S , Monaco , A P , Fisher , S E , Newbury , D F & SLI Consortium 2014 , ' Genome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairment ' , Genes, Brain, and Behavior , vol. 13 , no. 4 , pp. 418-429 . https://doi.org/10.1111/gbb.12127en
dc.identifier.issn1601-1848
dc.identifier.urihttp://hdl.handle.net/2164/4249
dc.descriptionFunded by •Medical Research Council. Grant Numbers: G1000569/1, MR/J003719/1, G0800523/86473 •University of Oxford Nuffield Department of Medicine Prize Studentship •Max Planck Society •Wellcome Trust. Grant Numbers: 060774, 076566, 090532/Z/09/Z, 092731 •National Institute of Health Research (UK) Senior Investigator award •Biomedical Research Centre in Mental Healthen
dc.format.extent12
dc.format.extent1025630
dc.language.isoeng
dc.relation.ispartofGenes, Brain, and Behavioren
dc.subjectALSPACen
dc.subjectGWASen
dc.subjectimprintingen
dc.subjectneurodevelopmental disorderen
dc.subjectspecific language impairmenten
dc.subjectattention-deficit/hyperactivity disorderen
dc.subjectnucleotide exchange factoren
dc.subjectRHO-GTPASESen
dc.subjectcommunication checklisten
dc.subjecthyperactivity disorderen
dc.subjectdevelopmental dyslexiaen
dc.subjectsusceptibility locusen
dc.subjectsuggestive linkageen
dc.subjectmental-retardationen
dc.subjectreading-disabilityen
dc.subjectR Medicineen
dc.subjectMedical Research Council (MRC)en
dc.subjectG1000569/1en
dc.subjectG0800523/86473en
dc.subjectMR/J003719/1en
dc.subjectWellcome Trusten
dc.subject060774en
dc.subject076566en
dc.subject090532/Z/09/Zen
dc.subject092731en
dc.subject.lccRen
dc.titleGenome- wide association analyses of child genotype effects and parent- of- origin effects in specific language impairmenten
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medical Educationen
dc.description.statusPeer revieweden
dc.identifier.doi10.1111/gbb.12127


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