Interstitial deletion del(17) (q21.3q23 or 24.2) syndrome

Clin Genet. 1993 Jan;43(1):54-5. doi: 10.1111/j.1399-0004.1993.tb04452.x.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 17*
  • Esophageal Atresia / genetics
  • Facial Bones / abnormalities
  • Female
  • Heart Defects, Congenital / genetics*
  • Humans
  • Hydrocephalus / genetics
  • Infant, Newborn
  • Male