A novel atypical 22q11.2 distal deletion in father and son

J Med Genet. 2002 Oct;39(10):E62. doi: 10.1136/jmg.39.10.e62.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Craniofacial Abnormalities / genetics
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Nuclear Family
  • Syndrome
  • Tetralogy of Fallot / genetics