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dc.contributor.authorAYCAN, Zehra
dc.contributor.authorPoyrazoglu, Sukran
dc.contributor.authorBas, Firdevs
dc.contributor.authorYILMAZ, Gulay Can
dc.contributor.authorAbali, Zehra Yavas
dc.contributor.authorSAVAS-ERDEVE, Senay
dc.contributor.authorCETINKAYA, Semra
dc.contributor.authorBerberoglu, Merih
dc.contributor.authorSiklar, Zeynep
dc.contributor.authorKorkmaz, Ozlem
dc.contributor.authorBULUS, Derya
dc.contributor.authorAkbas, Emine Demet
dc.contributor.authorGuran, Tulay
dc.contributor.authorBober, Ece
dc.contributor.authorAKIN, Onur
dc.date.accessioned2021-03-04T08:31:36Z
dc.date.available2021-03-04T08:31:36Z
dc.date.issued2017
dc.identifier.citationSAVAS-ERDEVE S., CETINKAYA S., Abali Z. Y. , Poyrazoglu S., Bas F., Berberoglu M., Siklar Z., Korkmaz O., BULUS D., Akbas E. D. , et al., "Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height", JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.30, sa.7, ss.759-766, 2017
dc.identifier.issn0334-018X
dc.identifier.othervv_1032021
dc.identifier.otherav_63bafd1b-eb1c-4940-aa1f-3d770f8d109e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/69421
dc.identifier.urihttps://doi.org/10.1515/jpem-2017-0088
dc.description.abstractBackground: The clinical, laboratory, genetic properties and final height of a large cohort of patients with nonclassical 21-hydroxylase deficiency (NC21OHD) in Turkey were analyzed.
dc.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.titleClinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
dc.contributor.departmentDr. Sami Ulus Education & Research Hospital , ,
dc.identifier.volume30
dc.identifier.issue7
dc.identifier.startpage759
dc.identifier.endpage766
dc.contributor.firstauthorID50662


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