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  5. Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/22597
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dc.contributor.authorManolakos, E.en
dc.contributor.authorVetro, A.en
dc.contributor.authorKefalas, K.en
dc.contributor.authorThomaidis, L.en
dc.contributor.authorAperis, G.en
dc.contributor.authorSotiriou, S.en
dc.contributor.authorKitsos, G.en
dc.contributor.authorMerkas, M.en
dc.contributor.authorSifakis, S.en
dc.contributor.authorPapoulidis, I.en
dc.contributor.authorLiehr, T.en
dc.contributor.authorZuffardi, O.en
dc.contributor.authorPetersen, M. B.en
dc.date.accessioned2015-11-24T19:25:16Z-
dc.date.available2015-11-24T19:25:16Z-
dc.identifier.issn1552-4833-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/22597-
dc.rightsDefault Licence-
dc.subjectAbnormalities, Multiple/genetics/*pathologyen
dc.subjectChild, Preschoolen
dc.subject*Chromosome Deletionen
dc.subjectChromosomes, Human, Pair 2/*geneticsen
dc.subjectComparative Genomic Hybridizationen
dc.subjectFemaleen
dc.subjectHumansen
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectIntellectual Disability/genetics/*pathologyen
dc.subjectKaryotypingen
dc.subjectMicrocephaly/genetics/*pathologyen
dc.subject*Phenotypeen
dc.titleDeletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardationen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1002/ajmg.a.33981-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/21567918-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/ajmg.a.33981/asset/33981_ftp.pdf?v=1&t=h09ozav2&s=86c1230a7f690343de9adfce0cfa13023d88cf7e-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2011-
heal.journalNameAm J Med Genet Aen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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