Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis

Clin Genet. 2003 Aug;64(2):168-71. doi: 10.1034/j.1399-0004.2003.00102.x.
No abstract available

Publication types

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

MeSH terms

  • Chromosomes, Human, Pair 22 / genetics*
  • Genetic Testing / methods*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Microsatellite Repeats / genetics*
  • Uniparental Disomy / genetics*