Unusual dicentric chromosome 22 associated with a 22q13 deletion

Am J Med Genet A. 2006 Dec 15;140(24):2819-23. doi: 10.1002/ajmg.a.31500.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Centromere / genetics
  • Child
  • Chromosome Banding
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Developmental Disabilities / genetics*
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Syndrome