Increased risk after noninvasive prenatal screening on cell-free DNA circulating in maternal blood: does a new indication for invasive prenatal diagnosis require new criteria for confirmatory cytogenetic analysis?

Prenat Diagn. 2015 Mar;35(3):308-9. doi: 10.1002/pd.4483.
No abstract available

Publication types

  • Letter

MeSH terms

  • Amniocentesis
  • Amnion / cytology
  • Chorionic Villi Sampling
  • Chromosome Disorders / diagnosis
  • Chromosome Disorders / genetics
  • Chromosomes, Human, Pair 13 / genetics
  • Chromosomes, Human, Pair 18 / genetics
  • Cytogenetic Analysis / methods*
  • DNA / blood*
  • Down Syndrome / diagnosis
  • Down Syndrome / genetics
  • Female
  • Fetus / metabolism*
  • Humans
  • Mosaicism
  • Pregnancy
  • Prenatal Diagnosis
  • Trisomy / diagnosis*
  • Trisomy / genetics
  • Trisomy 13 Syndrome
  • Trisomy 18 Syndrome
  • Turner Syndrome / diagnosis*
  • Turner Syndrome / genetics

Substances

  • DNA