Original Article

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations
  • Aslı Derya Kardelen
  • Güven Toksoy
  • Firdevs Baş
  • Zehra Yavaş Abalı
  • Genco Gençay
  • Şükran Poyrazoğlu
  • Rüveyde Bundak
  • Umut Altunoğlu
  • Şahin Avcı
  • Adam Najaflı
  • Oya Uyguner
  • Birsen Karaman
  • Seher Başaran
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2018; 10: 206-215 DOI: 10.4274/jcrpe.0032 PMID:29595516

Other

46,XY Complete Gonadal Dysgenesis: A Case Report
  • Hüseyin Anıl Korkmaz
  • Melek Yıldız
  • Filiz Hazan
  • Korcan Demir
  • Selma Tunç
  • Özlem Nalbantoğlu Elmas
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2015; 7: 65-65

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