Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19914
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dc.contributor.authorVermeesch, J. R.en
dc.contributor.authorSyrrou, M.en
dc.contributor.authorSalden, I.en
dc.contributor.authorDhondt, F.en
dc.contributor.authorMatthijs, G.en
dc.contributor.authorFryns, J. P.en
dc.date.accessioned2015-11-24T19:03:35Z-
dc.date.available2015-11-24T19:03:35Z-
dc.identifier.issn1468-6244-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19914-
dc.rightsDefault Licence-
dc.subjectAbnormalities, Multiple/genetics/pathologyen
dc.subject*Chromosome Aberrationsen
dc.subject*Chromosome Inversionen
dc.subjectCraniofacial Abnormalitiesen
dc.subjectFemaleen
dc.subjectGene Duplicationen
dc.subjectHumansen
dc.subjectIn Situ Hybridization, Fluorescenceen
dc.subjectInfanten
dc.subjectKaryotypingen
dc.subjectMicrocephaly/pathologyen
dc.subjectMosaicism/*geneticsen
dc.subjectPsychomotor Disorders/pathologyen
dc.titleMosaicism for duplication 12q (12q13-->12q21.2) accompanied by a pericentric inversion in a dysmorphic female infanten
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/12414834-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2002-
heal.journalNameJ Med Geneten
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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