dc.contributor.author | AYCAN, Zehra | |
dc.contributor.author | Poyrazoglu, Sukran | |
dc.contributor.author | Bas, Firdevs | |
dc.contributor.author | YILMAZ, Gulay Can | |
dc.contributor.author | Abali, Zehra Yavas | |
dc.contributor.author | SAVAS-ERDEVE, Senay | |
dc.contributor.author | CETINKAYA, Semra | |
dc.contributor.author | Berberoglu, Merih | |
dc.contributor.author | Siklar, Zeynep | |
dc.contributor.author | Korkmaz, Ozlem | |
dc.contributor.author | BULUS, Derya | |
dc.contributor.author | Akbas, Emine Demet | |
dc.contributor.author | Guran, Tulay | |
dc.contributor.author | Bober, Ece | |
dc.contributor.author | AKIN, Onur | |
dc.date.accessioned | 2021-03-04T08:31:36Z | |
dc.date.available | 2021-03-04T08:31:36Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | SAVAS-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.issn | 0334-018X | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_63bafd1b-eb1c-4940-aa1f-3d770f8d109e | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/69421 | |
dc.identifier.uri | https://doi.org/10.1515/jpem-2017-0088 | |
dc.description.abstract | Background: 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.iso | eng | |
dc.subject | İç Hastalıkları | |
dc.subject | Endokrinoloji ve Metabolizma Hastalıkları | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Tıp | |
dc.subject | PEDİATRİ | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | ENDOKRİNOLOJİ VE METABOLİZMA | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.title | Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | |
dc.contributor.department | Dr. Sami Ulus Education & Research Hospital , , | |
dc.identifier.volume | 30 | |
dc.identifier.issue | 7 | |
dc.identifier.startpage | 759 | |
dc.identifier.endpage | 766 | |
dc.contributor.firstauthorID | 50662 | |