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A prenatal case of a 46,XX[44]/48,XX,+2XMAR[11].ish(D14Z1/D22Z1+,WCP+)mat karyotype, with marker chromosome effects on the phenotypes in three generations

dc.contributor.authorTurkover, B.
dc.contributor.authorToksoy, G.
dc.contributor.authorYardimci, T.
dc.contributor.authorSahinoglu, Z.
dc.contributor.authorSayar, Sayar
dc.date.accessioned2021-03-05T08:14:17Z
dc.date.available2021-03-05T08:14:17Z
dc.identifier.citationSayar S., Toksoy G., Turkover B., Yardimci T., Sahinoglu Z., "A prenatal case of a 46,XX[44]/48,XX,+2XMAR[11].ish(D14Z1/D22Z1+,WCP+)mat karyotype, with marker chromosome effects on the phenotypes in three generations", 6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.122
dc.identifier.othervv_1032021
dc.identifier.otherav_97cf1489-0b2a-45ca-81e6-d085156dd3a1
dc.identifier.urihttp://hdl.handle.net/20.500.12627/102187
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.titleA prenatal case of a 46,XX[44]/48,XX,+2XMAR[11].ish(D14Z1/D22Z1+,WCP+)mat karyotype, with marker chromosome effects on the phenotypes in three generations
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume15
dc.contributor.firstauthorID99398


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