Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations

J Med Genet. 2003 Sep;40(9):690-6. doi: 10.1136/jmg.40.9.690.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Chromosome Deletion
  • Chromosome Disorders / genetics
  • Chromosome Disorders / pathology
  • Chromosomes, Human, Pair 20 / genetics*
  • Developmental Disabilities / pathology
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Male
  • Mental Disorders / pathology
  • Monosomy
  • Ring Chromosomes
  • Telomere / genetics*
  • Translocation, Genetic