Absence of a del(22q11) in a patient with the 3C (craniocerebellocardiac) syndrome

J Med Genet. 1998 Apr;35(4):347-8. doi: 10.1136/jmg.35.4.347-a.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Cerebellum / abnormalities*
  • Child, Preschool
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Craniofacial Abnormalities / genetics*
  • Female
  • Heart Septal Defects, Atrial / genetics*
  • Humans