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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.date.accessioned2018-06-29T15:51:47Z
dc.date.available2018-06-29T15:51:47Z
dc.date.issued2015-09
dc.identifierER3669
dc.identifier.citationCeroni, F., Simpson, N., Francks, C., Baird, G., Conti-Ramsden, G., Clark, A., Bolton, P., Hennessy, E., Donnelly, P., Bentley, D., Martin, H., Parr, J., Pagnamenta, A., Maestrini, E., Bacchelli, E., Fisher, S. & Newbury, D. (2015) Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis', European Journal of Human Genetics, vol. 23, , pp. 1113-1115,
dc.identifier.issn1018-4813
dc.identifier.urihttp://dx.doi.org/10.1038/ejhg.2014.275
dc.identifier.urihttps://eresearch.qmu.ac.uk/handle/20.500.12289/3669
dc.format.extent1113-1115
dc.relation.ispartofEuropean Journal of Human Genetics
dc.titleReply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis'
dc.typearticle
dcterms.accessRightsrestricted
dc.description.facultycasl
dc.description.volume23
dc.identifier.doihttp://doi:10.1038/ejhg.2014.275
dc.description.ispublishedpub
dc.description.eprintid3669
rioxxterms.typearticle
qmu.authorClark, Ann
qmu.centreCASL
qmu.centreCASLen
dc.description.statuspub
dc.description.number9


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