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dc.contributor.authorGallagher, Louiseen
dc.date.accessioned2018-08-23T11:14:01Z
dc.date.available2018-08-23T11:14:01Z
dc.date.issued2019en
dc.date.submitted2019en
dc.identifier.citationAl Shehhi, M. and Forman, E.B. and Fitzgerald, J.E. and McInerney, V. and Krawczyk, J. and Shen, S. and Betts, D.R. and Ardle, L.M. and Gorman, K.M. and King, M.D. and Green, A. and Gallagher, L. and Lynch, S.A., NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families, European Journal of Medical Genetics, 62, 3, 2019, 204-209en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/83971
dc.descriptionPUBLISHEDen
dc.descriptioncited By 0; Article in Pressen
dc.format.extent204-209en
dc.relation.ispartofseriesEuropean Journal of Medical Geneticsen
dc.relation.ispartofseries62en
dc.relation.ispartofseries3en
dc.rightsYen
dc.titleNRXN1 deletion syndrome; phenotypic and penetrance data from 34 familiesen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/lgallaghen
dc.identifier.rssinternalid191422en
dc.identifier.doihttp://dx.doi.org/10.1016/j.ejmg.2018.07.015en
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0001-9462-2836en


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