Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypes

J Med Genet. 2004 Jun;41(6):433-9. doi: 10.1136/jmg.2003.017202.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Breakage
  • Chromosome Deletion*
  • Chromosome Disorders / genetics
  • Chromosome Disorders / pathology
  • Chromosome Mapping
  • Chromosomes, Human, Pair 2 / genetics*
  • Female
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Microsatellite Repeats
  • Monosomy*
  • Phenotype