Non-invasive prenatal molecular detection of a fetal point mutation for congenital adrenal hyperplasia using co-amplification at lower denaturation temperature PCR

Chin Med J (Engl). 2010 Nov;123(22):3343-6.
No abstract available

MeSH terms

  • Adrenal Hyperplasia, Congenital / genetics*
  • Chromatography, High Pressure Liquid
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Female
  • Humans
  • Point Mutation / genetics*
  • Polymerase Chain Reaction / methods*
  • Pregnancy

Substances

  • CTGCAG-specific type II deoxyribonucleases
  • Deoxyribonucleases, Type II Site-Specific