Publication:
Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency

dc.contributor.authorGÜRAN, TÜLAY
dc.contributor.authorKARA, CENGİZ
dc.contributor.authorATAY, ZEYNEP
dc.contributor.authorAKBARZADE, AZAD
dc.contributor.authorYILMAZ, GÜLAY
dc.contributor.authorÇELEBİ BİTKİN, EDA
dc.contributor.authorAKÇAY, TEOMAN
dc.contributor.authorYILDIZ, MELEK
dc.contributor.authorGÜVEN, AYLA
dc.contributor.authorÇATLI, GÖNÜL
dc.contributor.authorYEŞİL, GÖZDE
dc.contributor.authorBAS, SERPİL
dc.contributor.authorVATANSEVER, PINAR
dc.contributor.authorHAKLAR, GONCAGÜL
dc.contributor.authorŞİRİKÇİ, ÖNDER
dc.contributor.authorTURAN, SERAP
dc.contributor.authorBEREKET, ABDULLAH
dc.contributor.institutionauthorYEŞİL, GÖZDE
dc.date.accessioned2019-11-17T23:44:08Z
dc.date.available2019-11-17T23:44:08Z
dc.date.issued2017-07-30
dc.identifier.citationGÜRAN T., KARA C., ATAY Z., AKBARZADE A., YILMAZ G., ÇELEBİ BİTKİN E., AKÇAY T., YILDIZ M., GÜVEN A., ÇATLI G., et al., -Evaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency-, American Association of Clinical Chemistry Congress, 30 July - 03 August 2017
dc.identifier.urihttps://hdl.handle.net/20.500.12645/10448
dc.language.isoen
dc.titleEvaluation of Clinical, Genetical, and Steroid Profile Features of Cases with 3Beta-Hydroxysteroid Dehydrogenase Type 2 Deficiency
dc.typeConference Paper
dspace.entity.typePublication
local.avesis.idd07aebf5-8d3e-41f4-96d2-a1152bd767ad
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relation.isAuthorOfPublication.latestForDiscoveryb653abbc-327a-4b3b-a227-f3344d8d6b70
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