Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker

Prenat Diagn. 2009 Dec;29(12):1177-9. doi: 10.1002/pd.2381.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Chromosomes, Human, Pair 18*
  • Female
  • Genetic Markers* / physiology
  • Genetic Testing / methods
  • Humans
  • In Situ Hybridization, Fluorescence / methods*
  • Inheritance Patterns
  • Pregnancy
  • Prenatal Diagnosis / methods*
  • Trisomy / diagnosis
  • Trisomy / genetics

Substances

  • Genetic Markers