Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4515
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dc.contributor.authorYildirim, B.-
dc.contributor.authorSemerci, C.N.-
dc.contributor.authorYa?ci, B.-
dc.contributor.authorDuman, K.-
dc.contributor.authorDüzcan, F.-
dc.date.accessioned2019-08-16T11:34:34Z-
dc.date.available2019-08-16T11:34:34Z-
dc.date.issued2006-
dc.identifier.issn1016-5126-
dc.identifier.urihttps://hdl.handle.net/11499/4515-
dc.description.abstractThe MURCS (MUllerian duct aplasia, Renal aplasia, Cervicothoracic Somite dysplasia) association is a rare and sporadic disease. The etiology is unknown. We present a patient with short stature, absence of uterus, tubes, left ovary, left renal agenesis, servical block vertebra.en_US
dc.language.isotren_US
dc.relation.ispartofJinekoloji ve Obstetrik Dergisien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMURCS associationen_US
dc.subjectagenesis and aplasiaen_US
dc.subjectarticleen_US
dc.subjectcase reporten_US
dc.subjectcervical spineen_US
dc.subjectfemaleen_US
dc.subjecthumanen_US
dc.subjectkidney agenesisen_US
dc.subjectMuellerian ducten_US
dc.subjectovary diseaseen_US
dc.subjectradiodiagnosisen_US
dc.subjectshort statureen_US
dc.subjectuterus malformationen_US
dc.subjectvagina aplasiaen_US
dc.titleOvarian agenesis and MURCS associationen_US
dc.typeArticleen_US
dc.identifier.volume20en_US
dc.identifier.issue3en_US
dc.identifier.startpage187
dc.identifier.startpage187en_US
dc.identifier.endpage189en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-33750627776en_US
dc.identifier.scopusqualityQ4-
dc.ownerPamukkale_University-
item.fulltextNo Fulltext-
item.languageiso639-1tr-
item.openairetypeArticle-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
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