Case Report

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
  • Assimina Galli Tsinopoulou
  • Anastasios Serbis
  • Eleni P. Kotanidou
  • Eleni Litou
  • Vaia Dokousli
  • Konstantina Mouzaki
  • Pavlos Fanis
  • Vassos Neocleous
  • Nicos Skordis
J Clin Res Pediatr Endocrinol 2018; 10: 74-78 DOI: 10.4274/jcrpe.4829 PMID:28739554
Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene
  • Ayfer Alikaşifoğlu
  • Doğuş Vurallı
  • Olaf Hiort
  • Nazlı Gönç
  • Alev Özön
  • Nurgün Kandemir
J Clin Res Pediatr Endocrinol 2015; 7: 249-252 DOI: 10.4274/jcrpe.2069 PMID:26831562