Prenatal diagnosis of compound heterozygous deficiency of protein C by direct detection of the mutation sites

Thromb Haemost. 1996 Aug;76(2):277-8.
No abstract available

Publication types

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

MeSH terms

  • Genetic Testing*
  • Heterozygote*
  • Humans
  • Infant, Newborn
  • Mutation
  • Prenatal Diagnosis*
  • Protein C / genetics*
  • Protein C Deficiency

Substances

  • Protein C