Case Report

CYP24A1 Mutation in a Girl Infant with Idiopathic Infantile Hypercalcemia
  • Jens Otto Broby Madsen
  • Sabrina Sauer
  • Bodo Beck
  • Jesper Johannesen
J Clin Res Pediatr Endocrinol 2018; 10: 83-86 DOI: 10.4274/jcrpe.4841 PMID:28874334

Original Article

SLC34A3 Intronic Deletion in a New Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria
  • Shirin Hasani-Ranjbar
  • Mahsa M. Amoli
  • Azadeh Ebrahim-Habibi
  • Ehsan Dehghan
  • Akbar Soltani
  • Parvin Amiri
  • Bagher Larijani
J Clin Res Pediatr Endocrinol 2012; 4: 89-93 DOI: 10.4274/jcrpe.601 PMID:22672866

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