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Polyorchism: a Case Report

dc.authorscopusid 8855691800
dc.authorscopusid 56363775800
dc.authorscopusid 8855691600
dc.contributor.author Polat, F.R.
dc.contributor.author Özer, A.
dc.contributor.author Polat, S.
dc.date.accessioned 2025-05-10T17:06:15Z
dc.date.available 2025-05-10T17:06:15Z
dc.date.issued 2003
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Polat F.R., Department of Surgery, State Hospital, Van, Turkey, Arastirma Hastnesi Arkasi, Van, Kardelen sitesi, C-Blok no. 5, Turkey; Özer A., Department of Surgery, State Hospital, Van, Turkey; Polat S., Department of Pathology, Medicine Faculty, 100 Year University, Van, Turkey en_US
dc.description.abstract Background: Polyorchism is a rare anomaly whose genesis is unclarified, although several theories have been proposed. It is generally associated with other disorders but seldom with malignancy. Conclusions: When a supernumerary testicle is encountered intraoperatively, it should be removed. © 2004 Kluwer Academic Publishers. en_US
dc.identifier.doi 10.1023/B:UROL.0000020266.94430.15
dc.identifier.endpage 254 en_US
dc.identifier.issn 0301-1623
dc.identifier.issue 2 en_US
dc.identifier.pmid 15072505
dc.identifier.scopus 2-s2.0-12144285701
dc.identifier.scopusquality Q2
dc.identifier.startpage 253 en_US
dc.identifier.uri https://doi.org/10.1023/B:UROL.0000020266.94430.15
dc.identifier.uri https://hdl.handle.net/20.500.14720/6370
dc.identifier.volume 35 en_US
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.relation.ispartof International Urology and Nephrology en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Inguinal Hernia en_US
dc.subject Polyorchism en_US
dc.title Polyorchism: a Case Report en_US
dc.type Article en_US

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