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dc.contributor.authorKara N.
dc.contributor.authorÖkten G.
dc.contributor.authorGüneş S.Ö.
dc.contributor.authorKoçak I.
dc.contributor.authorYiğit S.
dc.contributor.authorTural Ş.
dc.contributor.authorPinarli F.A.
dc.date.accessioned2020-06-21T09:23:25Z
dc.date.available2020-06-21T09:23:25Z
dc.date.issued2005
dc.identifier.issn1300-2996
dc.identifier.urihttps://hdl.handle.net/20.500.12712/3546
dc.description.abstractIn this study, we aimed to present of the results cytogenetic analysis and amniocentesis indications between the years 2000 and 2005 at Samsun and around. In this study 530 pregnancies were investigated. Each patient had one of the amniocentesis indications such as high biochemical risk (?1/250), mother age (?35), genetic disease in the family history, abnormal ultrasonography findings, and combination of indications given above. Amnion samples were analyzed with conventional cytogenetic methods in weeks 16-20 of conceptions. Average age of mothers in the study was 34.6 years old. Amnion samples chromosome analyses, showed 2.7% anomalies. These are 0.9% classic trisomy 21, 0.2% mosaic, 0.8% balanced translocations, and 0.8% pericentric inversions.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAmniocentesis indicationsen_US
dc.subjectPrenatal diagnosisen_US
dc.subjectResults of cytogenetic analysisen_US
dc.titleResults of amniocentesis cytogenetic analysis between 2000 and 2005 years at Samsun and arounden_US
dc.title.alternativeSamsun ve çevresinde 2000-2005 yillari arasinda amniyosentez sitogenetik analiz sonuçlarien_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume22en_US
dc.identifier.issue3en_US
dc.identifier.startpage119en_US
dc.identifier.endpage122en_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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