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Disruption of HDX gene in premature ovarian failure

dc.contributor.authorOkten, Gulsen
dc.contributor.authorGunes, Sezgin
dc.contributor.authorOnat, Onur Emre
dc.contributor.authorTukun, Ajlan
dc.contributor.authorOzcelik, Tayfun
dc.contributor.authorKocak, Idris
dc.date.accessioned2020-06-21T14:05:00Z
dc.date.available2020-06-21T14:05:00Z
dc.date.issued2013
dc.identifier.issn1939-6368
dc.identifier.issn1939-6376
dc.identifier.urihttps://doi.org/10.3109/19396368.2013.769028
dc.identifier.urihttps://hdl.handle.net/20.500.12712/15757
dc.descriptionWOS: 000322021800007en_US
dc.descriptionPubMed: 23441923en_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.language.isoengen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.isversionof10.3109/19396368.2013.769028en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectHDX geneen_US
dc.subjectpremature ovarian failureen_US
dc.subjectX chromosome inactivationen_US
dc.subjectX;autosome translocationen_US
dc.titleDisruption of HDX gene in premature ovarian failureen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume59en_US
dc.identifier.issue4en_US
dc.identifier.startpage218en_US
dc.identifier.endpage222en_US
dc.relation.journalSystems Biology in Reproductive Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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