Improved detection of the sickle mutation by DNA analysis: application to prenatal diagnosis

N Engl J Med. 1982 Jul 1;307(1):32-6. doi: 10.1056/NEJM198207013070106.
No abstract available

Publication types

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

MeSH terms

  • Anemia, Sickle Cell / diagnosis*
  • Base Sequence
  • Beta-Globulins / genetics
  • DNA / analysis*
  • DNA Restriction Enzymes*
  • Deoxyribonucleases, Type II Site-Specific*
  • Female
  • Genetic Linkage
  • Humans
  • Male
  • Nucleic Acid Hybridization
  • Polymorphism, Genetic
  • Pregnancy
  • Prenatal Diagnosis / methods*

Substances

  • Beta-Globulins
  • DNA
  • DNA Restriction Enzymes
  • endodeoxyribonuclease MstII
  • Deoxyribonucleases, Type II Site-Specific