Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/18927
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dc.contributor.authorPampanos, A.en
dc.contributor.authorNeou, P.en
dc.contributor.authorIliades, T.en
dc.contributor.authorApostolopoulos, N.en
dc.contributor.authorVoyiatzis, N.en
dc.contributor.authorGrigoriadou, M.en
dc.contributor.authorKatsichti, L.en
dc.contributor.authorSkevas, A.en
dc.contributor.authorPetersen, M. B.en
dc.date.accessioned2015-11-24T18:55:46Z-
dc.date.available2015-11-24T18:55:46Z-
dc.identifier.issn0009-9163-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/18927-
dc.rightsDefault Licence-
dc.subjectAllelesen
dc.subjectConnexins/*geneticsen
dc.subjectFamily Healthen
dc.subjectFemaleen
dc.subject*Gene Deletionen
dc.subject*Genes, Dominanten
dc.subjectHearing Loss, Sensorineural/*geneticsen
dc.subjectHomozygoteen
dc.subjectHumansen
dc.subjectInfanten
dc.subjectMaleen
dc.subjectPedigreeen
dc.subjectPolymerase Chain Reactionen
dc.titlePseudodominant inheritance of DFNB1 deafness due to the common 35delG mutationen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/10782932-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1034/j.1399-0004.2000.570311.x/asset/j.1399-0004.2000.570311.x.pdf?v=1&t=h2d53fi0&s=cecbd145ccd5164907b99c89d18ce789c833e1ac-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2000-
heal.journalNameClin Geneten
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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