Letter to Editor

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy
  • Korcan Demir
  • Özlem Nalbantoğlu
  • Kadri Karaer
  • Hüseyin Anıl Korkmaz
  • Melek Yıldız
  • Selma Tunç
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2015; 7: 356-357 DOI: 10.4274/jcrpe.2597

Case Report

Brain Abscess in a Patient with Osteopetrosis: A Rare Complication
  • Merve İşeri Nepesov
  • Eylem Kıral
  • Gürkan Bozan
  • Ömer Kılıç
  • Kürşat Bora Çarman
  • Coşkun Yarar
  • Suzan Şaylısoy
  • Ener Çağrı Dinleyici
J Clin Res Pediatr Endocrinol 2021; 13: 358-361 DOI: 10.4274/jcrpe.galenos.2020.2020.0039 PMID:32840095
A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation
  • Sol Kang
  • Young Kyung Kang
  • Jun Ah Lee
  • Dong Ho Kim
  • Jung Sub Lim
J Clin Res Pediatr Endocrinol 2019; 11: 439-443 DOI: 10.4274/jcrpe.galenos.2019.2018.0229 PMID:30759959

Other

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Infantile Osteopetrosis
  • Korcan Demir
  • Özlem Nalbantoğlu Elmas
  • Kadri Karaer
  • Hüseyin Anıl Korkmaz
  • Melek Yıldız
  • Selma Tunç
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2015; 7: 76-76