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dc.contributor.authorDemir, Z.
dc.contributor.authorUyguner, O.
dc.contributor.authorKirmizi, N.
dc.contributor.authorKayserili, H.
dc.contributor.authorBasaran, S.
dc.contributor.authorYilmaz, K.
dc.contributor.authorKaraman, B.
dc.contributor.authorUzumcu, A.
dc.contributor.authorKocbas, A.
dc.date.accessioned2021-03-03T19:01:00Z
dc.date.available2021-03-03T19:01:00Z
dc.identifier.citationYilmaz K., Karaman B., Uzumcu A., Kocbas A., Kirmizi N., Demir Z., Uyguner O., Kayserili H., Basaran S., "A case with non-mosaic de novo monosomy Xp and trisomy Xq21.2 -> Xqter: paternal in origin", 6th European Cytogenetics Conference, İstanbul, Türkiye, 7 - 10 Temmuz 2007, cilt.15, ss.50
dc.identifier.othervv_1032021
dc.identifier.otherav_5246cfba-79d5-4d28-846e-189a59f8b2a0
dc.identifier.urihttp://hdl.handle.net/20.500.12627/58434
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 case with non-mosaic de novo monosomy Xp and trisomy Xq21.2 -> Xqter: paternal in origin
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume15
dc.contributor.firstauthorID132987


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