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dc.contributor.authorBesser, R E Jen
dc.contributor.authorFlanagan, Sarahen
dc.contributor.authorMackay, D G Jen
dc.contributor.authorTemple, I Ken
dc.contributor.authorShepherd, Maggieen
dc.contributor.authorShields, Beverleyen
dc.contributor.authorEllard, Sianen
dc.contributor.authorHattersley, Andrew T.en
dc.date.accessioned2016-09-06T13:45:04Z
dc.date.available2016-09-06T13:45:04Z
dc.date.issued2016-09
dc.identifier.citationPrematurity and Genetic Testing for Neonatal Diabetes. 2016, 138 (3): Pediatricsen
dc.identifier.issn1098-4275
dc.identifier.pmid27540106
dc.identifier.doi10.1542/peds.2015-3926
dc.identifier.urihttp://hdl.handle.net/11287/619912
dc.description.abstractHyperglycemia in premature infants is usually thought to reflect inadequate pancreatic development rather than monogenic neonatal diabetes. No studies, to our knowledge, have investigated the prevalence of monogenic forms of diabetes in preterm infants.en
dc.language.isoenen
dc.relation.urlhttp://pediatrics.aappublications.org/cgi/pmidlookup?view=long&pmid=27540106en
dc.rightsArchived with thanks to Pediatricsen
dc.subjectWessex Classification Subject Headings::Endocrinology::Diabetesen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titlePrematurity and Genetic Testing for Neonatal Diabetes.en
dc.typeJournal Articleen
dc.identifier.journalPediatricsen
dc.type.versionPublisheden


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