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dc.contributor.authorTürkyılmaz, Ayşegül
dc.contributor.authorAlp, M. Nail
dc.contributor.authorBudak, Turgay
dc.date.accessioned2020-05-20T13:46:56Z
dc.date.available2020-05-20T13:46:56Z
dc.date.issued2007
dc.identifier.citationTürkyılmaz, A., Alp, M.N. ve Budak, T. (2007). 481 Amniyosentez, koryon villus biyopsisi ve kordosentez örneğinin prenatal genetik tanısı. Dicle Tıp Dergisi, 34(3), 187-190.tr_TR
dc.identifier.issn1300-2945
dc.identifier.issn1308-9889
dc.identifier.urihttp://www.diclemedj.org/upload/sayi/56/Dicle%20Med%20J-02626.pdf
dc.identifier.urihttp://hdl.handle.net/11468/5511
dc.description.abstractBu çalışmada; 1999–2001 tarihleri arasında Dicle Üniversitesi Tıp Fakültesi Tıbbi Biyoloji A.D. Prenatal Tanı Laboratuvarına sitogenetik tanı amacıyla gönderilen Koryon Villi Örneklemesi(CVS), Amniyosentez (AS) ve Kordosentez (KS)’e ait toplam 481 örnek materyal değerlendirilmiştir. Toplam 24 örnekte anormal kromozom kuruluşu saptanmıştır. Bunlardan 11 örnekte Trizomi 21 (Down Sendromu), 2 örnekte 14 ve 21 nolu kromozomlar arasında Robertson tipi translokasyonlu Down Sendromu, 1 örnekte mozaik Down Sendromu, 1 örnekte dengeli translokasyon kromozomu taşıyıcılığı, 2 örnekte Turner Sendromu, 1 örnekte Triple X Sendromu, 2 örnekte Triploidi, 1 örnekte Parsiyel trizomi 3, 1 örnekte derivativ kromozom, 1 örnekte tekrarlamayan sayısal ve yapısal düzensizlik, 1 örnekte de marker kromozom kuruluşu saptanmıştır. 15 örnekte üreme olmamıştır. Yanlış pozitif -negatif sonucumuz yoktur.tr_TR
dc.description.abstractIn this study, we evaluated a total of 481 amniocentesis , cordocentesis and corion villi sample specimens from patients who were referred to the Prenatal Diagnostic Laboratory of Department of Medical Biology and Genetics Department of Medical Faculty of University of Dicle, between 1999 and 2001. A total of 24 specimens were found cytogenetically abnormal, of which 11 were trisomy 21 ( Down Syndrome), two were Down Syndrome with Robertsonian type of translocation between chromosome 14 and 21, one was mosaic Down Syndrome , one was balanced translocated chromosome carrier, two were Turner Syndrome, one was triple X syndrome, two were triploidy, one was partial trisomy 3, one was derivative chromosome, one was nonrepetitive numerical and structural abnormality, and one was marker chromosome. Unfortunately, we could not have results in 15 of culture samples.tr_TR
dc.language.isoturtr_TR
dc.publisherDicle Üniversitesi Tıp Fakültesitr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subjectPrenatal tanıtr_TR
dc.subjectKromozom analizitr_TR
dc.subjectPrenatal diagnosistr_TR
dc.subjectKromozom anomalisitr_TR
dc.subjectChromosome analysistr_TR
dc.subjectChromosomal abnormalitytr_TR
dc.title481 Amniyosentez, koryon villus biyopsisi ve kordosentez örneğinin prenatal genetik tanısıtr_TR
dc.title.alternativePrenatal genetic diagnosis in 481 amniocentesis, chorion villi sample and cordocentesis specimenstr_TR
dc.typeArticletr_TR
dc.identifier.volume34tr_TR
dc.identifier.issue3tr_TR
dc.identifier.startpage187tr_TR
dc.identifier.endpage190tr_TR
dc.relation.journalDicle Tıp Dergisitr_TR
dc.contributor.departmentDicle Üniversitesi, Tıp Fakültesi, Tıbbi Biyoloji ve Genetik Anabilim Dalıtr_TR
dc.contributor.authorID152896tr_TR
dc.relation.publicationcategoryUlusal Yayıntr_TR
dc.contributor.orcid0000-0002-0995-8704tr_TR


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