Case Report

Aromatase Deficiency in Two Siblings with 46, XX Karyotype Raised 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 PMID:30968679
A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation
  • Fatma Dursun
  • Serdar Ceylaner
J Clin Res Pediatr Endocrinol 2019; 11: 196-201 DOI: 10.4274/jcrpe.galenos.2018.2018.0140 PMID:30074481
Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene
  • Edip Unal
  • Ruken Yıldırım
  • Funda Feryal Taş
  • Vasfiye Demir
  • Hüseyin Onay
  • Yusuf Kenan Haspolat
J Clin Res Pediatr Endocrinol 2018; 10: 377-381 DOI: 10.4274/jcrpe.0011 PMID:29553041

Poster Presentations

A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation
  • Ümmet Abur
  • Ayşegül Atmaca
  • Hamish Scott
  • Lucia Gagliardi
  • Engin Altundağ
  • Ömer Salih Akar
  • ilkay Koray Bayrak
  • Gönül Oğur
J Clin Res Pediatr Endocrinol 2017; 9: 2-2

Case Report

Aromatase Deficiency, a Rare Syndrome: Case Report
  • Emine Kartal Baykan
  • Mehmet Erdoğan
  • Samim Özen
  • Şükran Darcan
  • L. Füsun Saygılı
J Clin Res Pediatr Endocrinol 2013; 5: 129-132 DOI: 10.4274/Jcrpe.970 PMID:23748068

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