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Mayer-Rokitansky-Kuster-Hauser syndrome associated with unilateral gonadal agenesis - A case report

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dc.creator Kaya, H
dc.creator Ozkaya, O
dc.creator Kose, SA
dc.creator Sezik, Mekin
dc.date 2003-10-31T22:00:00Z
dc.date.accessioned 2020-10-06T10:14:14Z
dc.date.available 2020-10-06T10:14:14Z
dc.identifier 54e9982d-0457-43f9-91fd-e014f0604a75
dc.identifier https://avesis.sdu.edu.tr/publication/details/54e9982d-0457-43f9-91fd-e014f0604a75/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/60390
dc.description BACKGROUND: Mayer-Rokitansky-Kuster-Hauser syndrome is the second most frequent cause of primary amenorrhea, with a reported incidence of 0.002%. Patients have a normal karyotype and usually normal ovaries. Associated ovarian abnormalities are rarely reported.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Mayer-Rokitansky-Kuster-Hauser syndrome associated with unilateral gonadal agenesis - A case report
dc.type info:eu-repo/semantics/article


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