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A common cause for a common phenotype : the gatekeeper hypothesis in fetal programming

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.contributor.institutionUniversity of Aberdeen.Rowett Instituteen
dc.date.accessioned2016-02-08T10:47:01Z
dc.date.available2016-02-08T10:47:01Z
dc.date.issued2012-01
dc.descriptionCopyright © 2011 Elsevier Ltd. All rights reserved.en
dc.description.statusPeer revieweden
dc.format.extent7
dc.format.extent627191
dc.identifier12625481
dc.identifierb3e29b0a-98c3-4d8a-877a-90b2d2da1b25
dc.identifier22047985
dc.identifier83155175110
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.doi10.1016/j.mehy.2011.09.047
dc.identifier.iss1en
dc.identifier.issn1532-2777
dc.identifier.urihttp://hdl.handle.net/2164/5494
dc.identifier.vol78en
dc.language.isoeng
dc.relation.ispartofMedical hypothesesen
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

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