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dc.contributor.authorMalatyalioglu E.
dc.contributor.authorYanik F.F.
dc.date.accessioned2020-06-21T09:16:02Z
dc.date.available2020-06-21T09:16:02Z
dc.date.issued1999
dc.identifier.issn1300-2996
dc.identifier.urihttps://hdl.handle.net/20.500.12712/2844
dc.description.abstractBased on elevated MSAFP levels, 85% to 90% of NTDs can be detected. Using a combination of the three parameters, MSAFP, hCG and UE3, 55% to 60% of fetal Down's syndrome can be detected. Future strategies for Down's syndrome screening may include the use of new markers such as dimeric inhibin-A and urinary ?-core fragment of hCG, as well as first-trimester screening, particularly with PAPP-A and free ?-hCG.en_US
dc.language.isoturen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject?-fetoproteinen_US
dc.subjectDown's syndromeen_US
dc.subjectHuman chorionic gonadotropinen_US
dc.subjectNeural tube defectsen_US
dc.subjectTriple markeren_US
dc.subjectUnconjugated estriolen_US
dc.titleMaternal serum screening for prenatal diagnosis of some fetal genetic disordersen_US
dc.title.alternativeBazi Fetal Genetik Hastaliklarin Prenatal Tanisinda Maternal Serum Taramasien_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume16en_US
dc.identifier.issue1en_US
dc.identifier.startpage76en_US
dc.identifier.endpage85en_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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