Case Report

Aromatase Deficiency in Two Siblings with 46, XX Karyotype Rraised as Different Genders: A Novel Mutation (p.R115X) in CYP19A1 Gene
  • Samim Ozen
  • Tahir Atik
  • Ozlem Korkmaz
  • Huseyin Onay
  • Damla Goksen
  • Ferda Ozkınay
  • Ozgur Cogulu
  • Sukran Darcan
J Clin Res Pediatr Endocrinol 0; 0: 0-0 [e-Pub] DOI: 10.4274/jcrpe.galenos.2019.2018.0198

Original Article

Nationwide Study of Turner Syndrome in Ukrainian Children: Prevalence, Genetic Variants and Phenotypic Features
  • Nataliya Zelinska
  • Iryna Shevchenko
  • Evgenia Globa
J Clin Res Pediatr Endocrinol 2018; 10: 256-263 DOI: 10.4274/jcrpe.5119 PMID:29537378

Case Report

Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype
  • Özge Yüce
  • Esra Döğer
  • Nurullah Çelik
  • Hamdi Cihan Emeksiz
  • Mahmut Orhun Çamurdan
  • Aysun Bideci
  • Peyami Cinaz
J Clin Res Pediatr Endocrinol 2015; 7: 336-339 DOI: 10.4274/jcrpe.2022 PMID:26777047

Other

A Case of Mosaic 45,X/46,XY Infertile Man with an AZF Deletion
  • Mine Balasar
  • Pelin Taşdemir
  • Özgür Balasar
  • Emine Göktaş
J Clin Res Pediatr Endocrinol 2015; 7: 77-77

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