Poster Presentations

Case Report of Leri-Weill Dyscontrosteosis Caused By SHOX Gene Deletion
  • Emel Hatun Aytaç Kaplan
  • Mehmet Keskin
  • Melda Melik
J Clin Res Pediatr Endocrinol 2017; 9: 14-14
A Case of SHOX Gene Deletion Diagnosed By Microarray
  • Erhan Parıltay
  • Esra Işık
  • Tahir Atik
  • Özgür Çoğulu
  • Ferda Özkınay
J Clin Res Pediatr Endocrinol 2017; 9: 20-20
Homozygous SHOX Gene Deletion Detected by Array-CGH in a Girl with Langer Mesomelic Dysplasia
  • Adam Najafli
  • Birsen Karaman
  • Bilge Nihan Satkin
  • Umut Altunoğlu
  • Oya Uyguner
  • Seher Başaran
J Clin Res Pediatr Endocrinol 2017; 9: 24-24

Original Research

Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature
  • Kenan Delil
  • Halil Gürhan Karabulut
  • Bülent Hacıhamdioğlu
  • Zeynep Şıklar
  • Merih Berberoğlu
  • Gönül Öçal
  • Ajlan Tükün
  • Hatice Ilgın Ruhi
J Clin Res Pediatr Endocrinol 2016; 8: 144-149 DOI: 10.4274/jcrpe.2307 PMID:26758084

Original Article

Detection of SHOX Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature
  • Semra Gürsoy
  • Filiz Hazan
  • Ayça Aykut
  • Özlem Nalbantoğlu
  • Hüseyin Anıl Korkmaz
  • Korcan Demir
  • Behzat Özkan
  • Özgür Çoğulu
J Clin Res Pediatr Endocrinol 2020; 12: 358-365 DOI: 10.4274/jcrpe.galenos.2020.2019.0001 PMID:32295321

About Journal

Forms

Useful Links

Applications