Detection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease [2]

Basit Öğe Kaydı
dc.contributor.authorAlpman A.
dc.contributor.authorBora E.
dc.contributor.authorKaraca E.
dc.contributor.authorCankaya T.
dc.contributor.authorOnay H.
dc.contributor.authorCogulu O.
dc.contributor.authorGunduz C.
dc.contributor.authorKleijer W.J.
dc.contributor.authorÖzkınay F.
dc.date.accessioned2019-10-27T00:22:31Z
dc.date.available2019-10-27T00:22:31Z
dc.date.issued2004
dc.departmentEge Üniversitesien_US
dc.description.abstract[No abstract available]en_US
dc.identifier.endpage100en_US
dc.identifier.issn1015-8146
dc.identifier.issue1en_US
dc.identifier.pmid15083708en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage99en_US
dc.identifier.urihttps://hdl.handle.net/11454/22607
dc.identifier.volume15en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofGenetic Counselingen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleDetection of trisomy 21 in a fetus during the investigation for Tay-Sachs disease [2]en_US
dc.typeLetteren_US

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu
PubMed İndeksli Yayın Koleksiyonu