dc.contributor.author | Demir, Korcan | |
dc.contributor.author | Ozkan, Behzat | |
dc.contributor.author | Tunc, Selma | |
dc.contributor.author | Yildiz, Melek | |
dc.contributor.author | Buyukinan, Muammer | |
dc.contributor.author | Nalbantoglu, Ozlem | |
dc.contributor.author | Korkmaz, Huseyin Anil | |
dc.date.accessioned | 2021-03-05T08:44:36Z | |
dc.date.available | 2021-03-05T08:44:36Z | |
dc.identifier.citation | Nalbantoglu 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.issn | 0334-018X | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_9a791c63-edf2-4858-a39c-3e17cdb37c29 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/103845 | |
dc.identifier.uri | https://doi.org/10.1515/jpem-2014-0501 | |
dc.description.abstract | Background: 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.iso | eng | |
dc.subject | Tıp | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | PEDİATRİ | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.subject | İç Hastalıkları | |
dc.subject | Endokrinoloji ve Metabolizma Hastalıkları | |
dc.subject | ENDOKRİNOLOJİ VE METABOLİZMA | |
dc.title | A novel mutation of AMH in three siblings with persistent Mullerian duct syndrome | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | |
dc.contributor.department | Izmir Dr Behcet Uz Children''s Disease & Surgery Training & Research Hospital , , | |
dc.identifier.volume | 28 | |
dc.identifier.startpage | 1379 | |
dc.identifier.endpage | 1382 | |
dc.contributor.firstauthorID | 2274017 | |