Publication:
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.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentÇocuk Cerrahi Ana Bilim Dalı
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.departmentÇocuk Endokrinoloji Ana Bilim Dalı
dc.contributor.researcheridAAG-8385-2021
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.
dc.identifier.endpage51
dc.identifier.issn0967-3849
dc.identifier.startpage51
dc.identifier.urihttp://hdl.handle.net/11452/22551
dc.identifier.volume13
dc.identifier.wos000205501400120
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSpringer
dc.relation.journalChromosome Research
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiochemistry & molecular biology
dc.subjectGenetics & heredity
dc.subject.wosBiochemistry & molecular biology
dc.subject.wosGenetics & heredity
dc.titleFamilial case of 46 XX male and 46 XX true hermaphrodite in the absence of SRY gene
dc.typeMeeting Abstract
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Çocuk Endokrinoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Çocuk Cerrahi Ana Bilim Dalı
local.indexed.atWOS

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