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dc.contributor.authorÖzdemir Ö.
dc.contributor.authorSüngü S.
dc.contributor.authorPerçin E.F.
dc.contributor.authorSezgin I.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T09:13:04Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T09:13:04Z
dc.date.issued2002
dc.identifier.issn0011-4545
dc.identifier.urihttps://dx.doi.org/10.1508/cytologia.67.135
dc.identifier.urihttps://hdl.handle.net/20.500.12418/4595
dc.description.abstractWe report 2 cases of complete androgen insensitivity syndrome from 1 family with 45,XY,t(13q;14q) karyotype including complete testicular feminisation (TF) clinical features. The chromosomal translocation is not generally considered part of the clinic spectrum in this group patients and most possibly it is the first report in the literature.en_US
dc.language.isoengen_US
dc.relation.isversionof10.1508/cytologia.67.135en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject45,XY,t(13q;14q) karyotypeen_US
dc.subjectTesticular feminisation syndromeen_US
dc.subjectTwo sibling reportsen_US
dc.titleComplete androgen insensitivity syndrome with 45,XY,t(13q;14q) translocation (two cases)en_US
dc.typearticleen_US
dc.relation.journalCytologiaen_US
dc.contributor.departmentÖzdemir, Ö., Department of Medical Biology, Faculty of Medicine, Cumhuriyet University, 58140-Sivas, Turkey -- Süngü, S., Department of Medical Biology, Faculty of Medicine, Cumhuriyet University, 58140-Sivas, Turkey -- Perçin, E.F., Department of Medical Biology, Faculty of Medicine, Cumhuriyet University, 58140-Sivas, Turkey -- Sezgin, I., Department of Medical Biology, Faculty of Medicine, Cumhuriyet University, 58140-Sivas, Turkeyen_US
dc.identifier.volume67en_US
dc.identifier.issue2en_US
dc.identifier.endpage137en_US
dc.identifier.startpage135en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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