Poster Presentations

FGFR2 Gene Mutations in Patients with Syndromic or Isolated Craniosynostosis
  • Emine Ipek Ceylan
  • Asli Ece Solmaz
  • Hüseyin Onay
  • Ayça Aykut
  • Asude Durmaz
  • Gözde Yesil
  • Filiz Hazan
  • Aslihan Kiraz
  • Beyhan Tüysüz
  • Meltem Cerrah Günes
J Clin Res Pediatr Endocrinol 2017; 9: 21-21

Case Report

Genoa Syndrome and Central Diabetes Insipidus: A Case Report
  • Bülent Hacıhamdioğlu
  • Zeynep Şıklar
  • Şenay Savaş Erdeve
  • Merih Berberoğlu
  • Gülhiz Deda
  • Serap Teber Tıraş
  • Suat Fitöz
  • Gönül Öçal
J Clin Res Pediatr Endocrinol 2010; 2: 89-91 DOI: 10.4274/jcrpe.v2i2.89 PMID:21274346

Letter to Editor

Crouzonodermoskeletal Syndrome with Hypoplasia of Corpus Callosum and Inferior Vermis
  • Fatih Gürbüz
  • Serdar Ceylaner
  • Ali Kemal Topaloğlu
  • Bilgin Yüksel
J Clin Res Pediatr Endocrinol 2016; 8: 373-374 DOI: 10.4274/jcrpe.3343

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