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Bir olgu nedeniyle turner sendromu ve literatürün gözden geçirilmesi

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dc.contributor.author Balat, Ayşe
dc.contributor.author Akıncı, Ayşehan
dc.contributor.author Turgut, Mehmet
dc.contributor.author Demirhan, Osman
dc.date.accessioned 2015-11-17T14:01:39Z
dc.date.available 2015-11-17T14:01:39Z
dc.date.issued 1997
dc.identifier.citation Balat, A., Akıncı, A.,Turgut, M.,Demirhan, O.,(1997). Bir olgu nedeniyle turner sendromu ve literatürün gözden geçirilmesi.Turgut Özal Tıp Merkezi Dergisi, 4 (4).449-452 ss. tr_TR
dc.identifier.uri http://www.totmdergisi.org/articles/1997/volume4/issue4/1997_4_4_18.pdf
dc.identifier.uri http://hdl.handle.net/11616/2701
dc.description [Journal of Turgut Ozal Medical Center 1997;4(4):449-452] tr_TR
dc.description.abstract Turner's syndrome (TS) is one of the most common chromosomal abnormalities with an estimated frequency among female live birth of 1/4000-8000. In this article, we presented a 4 month-old girl with 45, X0 karyotype. The literature about Turner's syndrome was reviewed. tr_TR
dc.description.abstract Turner's syndrome (TS) is one of the most common chromosomal abnormalities with an estimated frequency among female live birth of 1/4000-8000. In this article, we presented a 4 month-old girl with 45, X0 karyotype. The literature about Turner's syndrome was reviewed tr_TR
dc.language.iso tur tr_TR
dc.publisher İnönü Üniversitesi Tıp Fakültesi Dergisi tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.subject Turner sendromu tr_TR
dc.subject Büyüme geriliği tr_TR
dc.subject Turner syndrome tr_TR
dc.subject Growth retardation tr_TR
dc.title Bir olgu nedeniyle turner sendromu ve literatürün gözden geçirilmesi tr_TR
dc.title.alternative Turner s syndrome : a case report and review of the literature tr_TR
dc.type article tr_TR
dc.relation.journal Turgut Özal Tıp Merkezi Dergisi tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.contributor.authorID TR201700 tr_TR
dc.contributor.authorID TR10983 tr_TR
dc.identifier.volume 4 tr_TR
dc.identifier.issue 4 tr_TR
dc.identifier.startpage 449 tr_TR
dc.identifier.endpage 452 tr_TR


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