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Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21146
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dc.contributor.authorArtan, Sevilhan-
dc.contributor.authorBaşaran, Nurettin-
dc.contributor.authorHassa, Hikmet-
dc.contributor.authorÖzalp, S.-
dc.contributor.authorŞener, T.-
dc.contributor.authorSaylı, B.S.-
dc.contributor.authorÖzdemir, M.-
dc.contributor.authorDurak, T.-
dc.contributor.authorDolen, I.-
dc.contributor.authorÖzgünen, T.-
dc.contributor.authorTuna, M-
dc.date.accessioned2021-07-07T08:40:00Z-
dc.date.available2021-07-07T08:40:00Z-
dc.date.issued1995-
dc.identifier.citationArtan, S. vd. (1995). ''Confined placental mosaicism in term placentae: Analysis of 125 cases''. Prenatal Diagnosis, 15(12), 1135-1142.en_US
dc.identifier.issn0197-3851-
dc.identifier.urihttps://doi.org/10.1002/pd.1970151210-
dc.identifier.urihttps://obgyn.onlinelibrary.wiley.com/doi/10.1002/pd.1970151210-
dc.identifier.urihttp://hdl.handle.net/11452/21146-
dc.description.abstractIn order to determine the incidence of confined placental mosaicism (CPM) in term placentae and to show the presence of specific sites and the effect on fetal development, 125 placentae from uneventful pregnancies were analysed by cytogenetic methods. The incidence was at least 4.8 per cent and there were no specific sites on the placenta. Although the number of cases is still too small, we found CPM to be associated with intrauterine growth retardation in six cases.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley & Sonsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectConfined placental mosaicismen_US
dc.subjectIntrauterine growth retardationen_US
dc.subjectChorionic villusen_US
dc.subjectUniparental disomyen_US
dc.subjectChromosome mosaicismen_US
dc.subjectFollow-upen_US
dc.subjectAssociationen_US
dc.subjectTrisomy-16en_US
dc.subjectCVSen_US
dc.subjectConfirmationen_US
dc.subjectAccuracyen_US
dc.subjectGenetics & heredityen_US
dc.subjectObstetrics & gynecologyen_US
dc.titleConfined placental mosaicism in term placentae: Analysis of 125 casesen_US
dc.typeArticleen_US
dc.identifier.wosA1995TK68400007tr_TR
dc.identifier.scopus2-s2.0-0028876168tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı.tr_TR
dc.identifier.startpage1135tr_TR
dc.identifier.endpage1142tr_TR
dc.identifier.volume15tr_TR
dc.identifier.issue12tr_TR
dc.relation.journalPrenatal Diagnosistr_TR
dc.contributor.buuauthorCengiz, C.-
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed8750294tr_TR
dc.subject.wosGenetics & heredityen_US
dc.subject.wosObstetrics & gynecologyen_US
dc.indexed.wosSCIEtr_TR
dc.indexed.scopusScopustr_TR
dc.indexed.pubmedPubmedtr_TR
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