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Persistent mullerian duct syndrome - A case report

dc.contributor.authorElcioglu, N
dc.contributor.authorErk, A
dc.contributor.authorOzeren, S
dc.contributor.authorOzbay, O
dc.contributor.authorVural, B
dc.date.accessioned2021-03-03T14:50:56Z
dc.date.available2021-03-03T14:50:56Z
dc.date.issued1999
dc.identifier.citationErk A., Ozeren S., Ozbay O., Vural B., Elcioglu N., "Persistent mullerian duct syndrome - A case report", JOURNAL OF REPRODUCTIVE MEDICINE, cilt.44, sa.2, ss.135-138, 1999
dc.identifier.issn0024-7758
dc.identifier.othervv_1032021
dc.identifier.otherav_3bcc9f04-18b7-4097-a8a3-d9312982612e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/44145
dc.description.abstractBACKGROUND: Persistent mullerian duct syndrome is a rare form of male pseudohermaphroditism in which well-developed mullerian structures are present in an otherwise normal male with XY chromosomes. The syndrome was first described by Nilson in 1939, and almost 100 cases have been reported.
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectCerrahi Tıp Bilimleri
dc.subjectKadın Hastalıkları ve Doğum
dc.subjectKADIN HASTALIKLARI & DOĞUM
dc.titlePersistent mullerian duct syndrome - A case report
dc.typeMakale
dc.relation.journalJOURNAL OF REPRODUCTIVE MEDICINE
dc.contributor.department, ,
dc.identifier.volume44
dc.identifier.issue2
dc.identifier.startpage135
dc.identifier.endpage138
dc.contributor.firstauthorID122718


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