Publication:
Disruption of HDX Gene in Premature Ovarian Failure

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dc.authorscopusid18038193800
dc.authorscopusid6603432100
dc.authorscopusid15056549400
dc.authorscopusid6602994976
dc.authorscopusid7005424336
dc.authorscopusid21134879300
dc.contributor.authorÖkten, G.
dc.contributor.authorGüneş, S.
dc.contributor.authorOnat, O.E.
dc.contributor.authorTükün, A.
dc.contributor.authorOzcelik, T.
dc.contributor.authorKoçak, I.
dc.date.accessioned2020-06-21T14:05:00Z
dc.date.available2020-06-21T14:05:00Z
dc.date.issued2013
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Ökten] Gülsen, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Güneş] Sezgin Özgür, Department of Medical Biology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Onat] Onur Emre, Department of Molecular Biology and Genetics, Bilkent Üniversitesi, Ankara, Ankara, Turkey; [Tükün] Ajlan, Department of Medical Genetics, Ankara Üniversitesi, Ankara, Turkey; [Ozcelik] Tayfun, Department of Molecular Biology and Genetics, Bilkent Üniversitesi, Ankara, Ankara, Turkey; [Koçak] Idris, Department of Obstetrics and Gynecology, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractWe present a case of a 19-year-old phenotypically normal girl with premature ovarian failure. Cytogenetic analysis using G banding and fluorescence in situ hybridization (FISH) from cultured peripheral blood lymphocytes of the patient and the family revealed a de novo X;15 translocation and the imbalance to be 46,X,t(X;15)(Xpter → Xq21en_US
dc.identifier.doi10.3109/19396368.2013.769028
dc.identifier.endpage222en_US
dc.identifier.issn1939-6368
dc.identifier.issn1939-6376
dc.identifier.issue4en_US
dc.identifier.pmid23441923
dc.identifier.scopus2-s2.0-84880690277
dc.identifier.scopusqualityQ2
dc.identifier.startpage218en_US
dc.identifier.urihttps://doi.org/10.3109/19396368.2013.769028
dc.identifier.volume59en_US
dc.identifier.wosWOS:000322021800007
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofSystems Biology in Reproductive Medicineen_US
dc.relation.journalSystems Biology in Reproductive Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHDX Geneen_US
dc.subjectPremature Ovarian Failureen_US
dc.subjectX Chromosome Inactivationen_US
dc.subjectXen_US
dc.subjectAutosome Translocationen_US
dc.titleDisruption of HDX Gene in Premature Ovarian Failureen_US
dc.typeArticleen_US
dspace.entity.typePublication

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