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dc.contributor.authorErgene, H
dc.contributor.authorHas, Recep
dc.contributor.authorErmis, H
dc.contributor.authorBasaran, Seher
dc.contributor.authorIbrahimoglu, L
dc.date.accessioned2021-03-04T14:14:37Z
dc.date.available2021-03-04T14:14:37Z
dc.date.issued2002
dc.identifier.citationHas R., Ibrahimoglu L., Ergene H., Ermis H., Basaran S., "Partial molar appearance of the placenta in trisomy 13.", Fetal diagnosis and therapy, cilt.17, sa.4, ss.205-8, 2002
dc.identifier.issn1015-3837
dc.identifier.otherav_807badf5-a645-4f29-b0dc-6419538eef07
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/87652
dc.identifier.urihttps://doi.org/10.1159/000059371
dc.description.abstractAlthough molecular studies have shown that more than 90% of partial moles are secondary to diandric triploidy, there are some rare cases with tetraploidy or unspecified aneuploidies. We diagnosed 3 cases of partial mole presentation during the 2nd trimester of pregnancy with multiple fetal abnormalities. In all 3 cases, cytogenetic studies showed trisomy 13, We present the cases and discuss the clinical and pathological aspects of the conditions presented as partial moles. Copyright (C) 2002 S. Karger AG, Basel.
dc.language.isoeng
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectCerrahi Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.titlePartial molar appearance of the placenta in trisomy 13.
dc.typeMakale
dc.relation.journalFetal diagnosis and therapy
dc.contributor.department, ,
dc.identifier.volume17
dc.identifier.issue4
dc.identifier.startpage205
dc.identifier.endpage8
dc.contributor.firstauthorID165342


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