Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19128
Full metadata record
DC FieldValueLanguage
dc.contributor.authorManolakos, E.en
dc.contributor.authorSifakis, S.en
dc.contributor.authorSotiriou, S.en
dc.contributor.authorPeitsidis, P.en
dc.contributor.authorEleftheriades, M.en
dc.contributor.authorMersinias, V.en
dc.contributor.authorLiehr, T.en
dc.contributor.authorThomaidis, L.en
dc.contributor.authorKitsos, G.en
dc.contributor.authorPapoulidis, I.en
dc.contributor.authorPetersen, M. B.en
dc.contributor.authorOrru, S.en
dc.date.accessioned2015-11-24T18:57:03Z-
dc.date.available2015-11-24T18:57:03Z-
dc.identifier.issn1473-5717-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19128-
dc.rightsDefault Licence-
dc.titlePrenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literatureen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1097/MCD.0b013e32834e9279-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/22391621-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2012-
heal.journalNameClin Dysmorpholen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

Files in This Item:
There are no files associated with this item.


This item is licensed under a Creative Commons License Creative Commons