Familial case of 46 XX male and 46 XX true hermaphrodite in the absence of SRY gene

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dc.contributor.buuauthorTemel, Sehime
dc.contributor.buuauthorGülten, Tuna
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.buuauthorSağlam, Halil
dc.contributor.buuauthorKılıç, Nizamettin
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Endokrinoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Çocuk Cerrahi Anabilim Dalı.tr_TR
dc.contributor.researcheridAAG-8385-2021tr_TR
dc.date.accessioned2021-11-02T08:50:05Z
dc.date.available2021-11-02T08:50:05Z
dc.date.issued2005
dc.identifier.citationTemel, S. vd. (2005). "Familial case of 46 XX male and 46 XX true hermaphrodite in the absence of SRY gene". Chromosome Research, 13, 51-51.en_US
dc.identifier.endpage51tr_TR
dc.identifier.issn0967-3849
dc.identifier.startpage51tr_TR
dc.identifier.urihttp://hdl.handle.net/11452/22551
dc.identifier.volume13tr_TR
dc.identifier.wos000205501400120tr_TR
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.journalChromosome Researchen_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararasıtr_TR
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiochemistry & molecular biologyen_US
dc.subjectGenetics & heredityen_US
dc.subject.wosBiochemistry & molecular biologyen_US
dc.subject.wosGenetics & heredityen_US
dc.titleFamilial case of 46 XX male and 46 XX true hermaphrodite in the absence of SRY geneen_US
dc.typeMeeting Abstract
dc.wos.quartileQ2en_US

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