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Novel NLRP7 mutations in familial recurrent hydatidiform mole: are NLRP7 mutations a risk for recurrent reproductive wastage?

dc.contributor.authorGedikbaşı, Asuman
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorKaraman, V.
dc.contributor.authorAkbayır, O
dc.contributor.authorOzgur, H.
dc.contributor.authorÜlker, Volkan
dc.contributor.authorGurkan, H.
dc.contributor.authorTozkir, H.
dc.contributor.authorNumanoğlu, C.
dc.date.accessioned2021-03-02T22:15:34Z
dc.date.available2021-03-02T22:15:34Z
dc.date.issued2013
dc.identifier.citationÜlker V., Gurkan H., Tozkir H., Karaman V., Ozgur H., Numanoğlu C., Gedikbaşı A., Akbayır O., Uyguner Z. O. , "Novel NLRP7 mutations in familial recurrent hydatidiform mole: are NLRP7 mutations a risk for recurrent reproductive wastage?", EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, cilt.170, sa.1, ss.188-192, 2013
dc.identifier.issn0301-2115
dc.identifier.othervv_1032021
dc.identifier.otherav_0bae41b6-242b-4b19-a675-822f78e1f23f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/13520
dc.identifier.urihttps://doi.org/10.1016/j.ejogrb.2013.06.028
dc.description.abstractObjective: Familial recurrent hydatidiform mole is an exceedingly rare clinical condition. Affected women are predisposed to molar pregnancies of diploid, biparental origin rather than androgenetic origin. At present, NLRP7 and KHDC3L (C6or (f) over bar 221) are the only genes known to be associated with familial recurrent hydatidiform mole. This study investigated the genetic dispositions in two large Turkish families with recurring molar conceptuses.
dc.language.isoeng
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectBiyoloji ve Biyokimya
dc.subjectÜREME BİYOLOJİSİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.titleNovel NLRP7 mutations in familial recurrent hydatidiform mole: are NLRP7 mutations a risk for recurrent reproductive wastage?
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY
dc.contributor.departmentIstanbul Kanuni Sultan Suleyman Training & Research Hospital , ,
dc.identifier.volume170
dc.identifier.issue1
dc.identifier.startpage188
dc.identifier.endpage192
dc.contributor.firstauthorID31147


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