Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion

J Med Genet. 1995 Aug;32(8):669. doi: 10.1136/jmg.32.8.669.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Child
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 22*
  • Cloning, Molecular
  • Cosmids
  • Female
  • Humans
  • Hypoparathyroidism / genetics*
  • Male