Publication:
Two Turner Syndrome Patients with the Mosaic 45,X/46,X,i(Xq) Karyotype: Case Report

dc.authorscopusid6603432100
dc.authorscopusid6603455076
dc.authorscopusid24333217100
dc.authorscopusid18038193800
dc.authorscopusid12805499100
dc.authorscopusid18038773000
dc.contributor.authorGüneş, S.
dc.contributor.authorKara, N.
dc.contributor.authorSürücü, B.
dc.contributor.authorÖkten, G.
dc.contributor.authorYigit, S.
dc.contributor.authorSezer, Ö.
dc.date.accessioned2025-12-10T21:33:30Z
dc.date.issued2008
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Güneş] Sezgin Özgür, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kara] Nurten, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Sürücü] Bülent, Samsun Kadin Hastaliklari ve Doǧumevi, Samsun, Turkey; [Ökten] Gülsen, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yigit] Serbulent, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Sezer] Ozlem Türkeli, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractTurner's syndrome is one of the most common chromosomal aneuploidy disorders. Turner's syndrome occurs in 1 in 4000 live-born girls and approximately 5 to 10 percent of them have mosaic isochromosome 45,X/46,X,i(Xq). Turner's syndrome is associated with reduced adult height and with gonadal dysgenesis, leading to insufficient circulating levels of female sex steroids and to infertility. In this study, we presented 18 year-old two girls having complaints of primary amenorrhea with mosaic 46,X,i(X)(qter→q10en_US
dc.identifier.endpage238en_US
dc.identifier.issn1300-0292
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-44349128984
dc.identifier.scopusqualityQ4
dc.identifier.startpage236en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12712/34722
dc.identifier.volume28en_US
dc.identifier.wosqualityN/A
dc.language.isotren_US
dc.publisherTurkiye Kliniklerien_US
dc.relation.ispartofTurkiye Klinikleri Journal of Medical Sciencesen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectIsochromosomesen_US
dc.subjectTurner Syndromeen_US
dc.titleTwo Turner Syndrome Patients with the Mosaic 45,X/46,X,i(Xq) Karyotype: Case Reporten_US
dc.title.alternative45,X/46,X,i(Xq) Karyotipe Sahip İki Mozaik Turner Sendromu Olgusuen_US
dc.typeArticleen_US
dspace.entity.typePublication

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