All Stories

  1. The Clinical Cases of Geleophysic Dysplasia: One Gene, Different Phenotypes
  2. Pharmacokinetics of IGF-I in PAPP-A2 Deficient Patients, Growth Response, and Effects on Glucose and Bone Density
  3. Paternally Inherited DLK1 Deletion Associated With Familial Central Precocious Puberty
  4. Clinical characterization of patients with autosomal dominant short stature due to aggrecan mutations
  5. AnXRCC4Splice Mutation Associated With Severe Short Stature, Gonadal Failure, and Early-Onset Metabolic Syndrome
  6. Idiopathic short stature due to novel heterozygous mutation of the aggrecan gene
  7. A Novel Variant inCDKN1CIs Associated With Intrauterine Growth Restriction, Short Stature, and Early-Adulthood-Onset Diabetes