Publication:
Premature Ovarian Failure and 46,X,del(X)(q21)

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dc.authorscopusid6603455076
dc.authorscopusid23471430800
dc.authorscopusid18038193800
dc.authorscopusid21134879300
dc.authorscopusid55174210700
dc.contributor.authorKara, N.
dc.contributor.authorTural, Ş.
dc.contributor.authorÖkten, G.
dc.contributor.authorKoçak, I.
dc.contributor.authorTekcan, A.
dc.date.accessioned2020-06-21T09:36:31Z
dc.date.available2020-06-21T09:36:31Z
dc.date.issued2012
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Kara] Nurten, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Tural] Şengül, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Ökten] Gülsen, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Koçak] Idris, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Tekcan] Akin, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractPremature ovarian failure (POF) is a common cause of infertility in women, and is characterised by amenorrhoea, hypo-oestrogenism and elevated gonadotrophin levels in women under the age of 40. Genetic, autoimmune and the environmental factors play a role in the pathogenesis. In this study, we investigated a 22 year-old woman having premature ovarian failure, referred to our laboratuary from Ondokuz Mayis University Gynecology and Obstetrics polyclinic. In conventional cytogenetic analysis, a deletion was observed in the long arm of the X chromosome 46,X,del(X)(q21). This finding was emphasised once again the significance of X chromosome deletions in the premature ovarian failure. © 2012 OMU.en_US
dc.identifier.doi10.5835/jecm.omu.29.02.018
dc.identifier.endpage168en_US
dc.identifier.issn1300-2996
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-84865483573
dc.identifier.startpage167en_US
dc.identifier.urihttps://doi.org/10.5835/jecm.omu.29.02.018
dc.identifier.urihttps://hdl.handle.net/20.500.12712/4449
dc.identifier.volume29en_US
dc.language.isotren_US
dc.relation.ispartofOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.journalOndokuz Mayis Universitesi Tip Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAmenorrheaen_US
dc.subjectChromosomal Aberrationen_US
dc.subjectCytogeneticsen_US
dc.subjectFemale Infertilityen_US
dc.subjectPremature Ovarian Failureen_US
dc.subjectX Chromosome Deletionen_US
dc.titlePremature Ovarian Failure and 46,X,del(X)(q21)en_US
dc.title.alternativePrematüre Ovaryen Yetmezlik ve 46,X,del(X)(q21)en_US
dc.typeArticleen_US
dspace.entity.typePublication

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