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A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome

dc.contributor.authorDemir, Korcan
dc.contributor.authorOzkan, Behzat
dc.contributor.authorTunc, Selma
dc.contributor.authorYildiz, Melek
dc.contributor.authorBuyukinan, Muammer
dc.contributor.authorNalbantoglu, Ozlem
dc.contributor.authorKorkmaz, Huseyin Anil
dc.date.accessioned2021-03-05T08:44:36Z
dc.date.available2021-03-05T08:44:36Z
dc.identifier.citationNalbantoglu O., Demir K., Korkmaz H. A. , Buyukinan M., Yildiz M., Tunc S., Ozkan B., "A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.28, ss.1379-1382, 2015
dc.identifier.issn0334-018X
dc.identifier.othervv_1032021
dc.identifier.otherav_9a791c63-edf2-4858-a39c-3e17cdb37c29
dc.identifier.urihttp://hdl.handle.net/20.500.12627/103845
dc.identifier.urihttps://doi.org/10.1515/jpem-2014-0501
dc.description.abstractBackground: Persistent Mullerian duct syndrome (PMDS) is a rare form of male 46, XY disorder of sex development characterized by the presence of Mullerian duct derivatives in otherwise phenotypically normal males.
dc.language.isoeng
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.titleA novel mutation of AMH in three siblings with persistent Mullerian duct syndrome
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
dc.contributor.departmentIzmir Dr Behcet Uz Children''s Disease & Surgery Training & Research Hospital , ,
dc.identifier.volume28
dc.identifier.startpage1379
dc.identifier.endpage1382
dc.contributor.firstauthorID2274017


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