Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation

J Med Genet. 2001 Feb;38(2):121-5. doi: 10.1136/jmg.38.2.121.
No abstract available

Publication types

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

MeSH terms

  • Blotting, Southern
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 1 / genetics*
  • DNA / genetics
  • DNA Probes
  • Female
  • Humans
  • In Situ Hybridization, Fluorescence
  • Intellectual Disability / genetics*
  • Male
  • Microsatellite Repeats / genetics*
  • Polymorphism, Genetic

Substances

  • DNA Probes
  • DNA