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Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism

dc.contributor.authorMengen, Eda
dc.contributor.authorBERBEROĞLU, MERİH
dc.contributor.authorOzbek, Mehmet Nuri
dc.contributor.authorDemirbilek, Huseyin
dc.contributor.authorKekil, M. Burcu
dc.contributor.authorTemiz, Fatih
dc.contributor.authorMungan, Neslihan Onenli
dc.contributor.authorYÜKSEL, BİLGİN
dc.contributor.authorTOPALOĞLU, ALİ KEMAL
dc.contributor.authorSaka, Nurcin
dc.contributor.authorGuven, Ayla
dc.contributor.authorPoyrazoglu, Sukran
dc.contributor.authorGÜRBÜZ, FATİH
dc.contributor.authorKOTAN, LEMAN DAMLA
dc.contributor.authorŞIKLAR, ZEYNEP
dc.contributor.authorDokmetas, Sebila
dc.contributor.authorKilicli, Mehmet Fatih
dc.contributor.authorKİREL, BİRGÜL
dc.contributor.authorCesur, Yasar
dc.contributor.authorDogan, Murat
dc.contributor.authorOzen, Samim
dc.date.accessioned2021-03-06T21:43:50Z
dc.date.available2021-03-06T21:43:50Z
dc.date.issued2012
dc.identifier.citationGÜRBÜZ F., KOTAN L. D. , Mengen E., ŞIKLAR Z., BERBEROĞLU M., Dokmetas S., Kilicli M. F. , Guven A., KİREL B., Saka N., et al., "Distribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism", JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY, cilt.4, ss.121-126, 2012
dc.identifier.issn1308-5727
dc.identifier.otherav_fffb6ad3-18fb-4762-8044-060660b31bf3
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/167337
dc.identifier.urihttps://doi.org/10.4274/jcrpe.725
dc.description.abstractObjective: Normosmic idiopathic hypogonadotropic hypogonadism (nIHH) is characterized by failure of initiation or maintenance of puberty due to insufficient gonadotropin release, which is not associated with anosmia/hyposmia. The objective of this study was to determine the distribution of causative mutations in a hereditary form of nIHH.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPEDİATRİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.titleDistribution of Gene Mutations Associated with Familial Normosmic Idiopathic Hypogonadotropic Hypogonadism
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY
dc.contributor.departmentÇukurova Üniversitesi , Tıp Fakültesi , Çocuk Sağlığı Ve Hastalıkları
dc.identifier.volume4
dc.identifier.issue3
dc.identifier.startpage121
dc.identifier.endpage126
dc.contributor.firstauthorID203217


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