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dc.contributor.authorMcMullen, S
dc.contributor.authorLangley-Evans, S C
dc.contributor.authorGambling, L
dc.contributor.authorLang, C
dc.contributor.authorSwali, A
dc.contributor.authorMcArdle, H J
dc.date.accessioned2016-02-08T10:47:01Z
dc.date.available2016-02-08T10:47:01Z
dc.date.issued2012-01
dc.identifier.citationMcMullen , S , Langley-Evans , S C , Gambling , L , Lang , C , Swali , A & McArdle , H J 2012 , ' A common cause for a common phenotype : the gatekeeper hypothesis in fetal programming ' , Medical hypotheses , vol. 78 , no. 1 , pp. 88-94 . https://doi.org/10.1016/j.mehy.2011.09.047en
dc.identifier.issn1532-2777
dc.identifier.otherPURE: 12625481
dc.identifier.otherPURE UUID: b3e29b0a-98c3-4d8a-877a-90b2d2da1b25
dc.identifier.otherPubMed: 22047985
dc.identifier.otherScopus: 83155175110
dc.identifier.urihttp://hdl.handle.net/2164/5494
dc.descriptionCopyright © 2011 Elsevier Ltd. All rights reserved.en
dc.format.extent7
dc.language.isoeng
dc.relation.ispartofMedical hypothesesen
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/en
dc.subjectSDG 3 - Good Health and Well-beingen
dc.subjectR Medicineen
dc.subject.lccRen
dc.titleA common cause for a common phenotype : the gatekeeper hypothesis in fetal programmingen
dc.typeJournal articleen
dc.contributor.institutionUniversity of Aberdeen.Medicine, Medical Sciences & Nutrition, Vascular Healthen
dc.contributor.institutionUniversity of Aberdeen.Rowett Instituteen
dc.description.statusPeer revieweden
dc.description.versionPublisher PDFen
dc.identifier.doihttps://doi.org/10.1016/j.mehy.2011.09.047
dc.identifier.vol78en
dc.identifier.iss1en


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