Application of a new DNA sequence polymorphism as a genetic marker in prenatal diagnosis of phenylketonuria

J Med Genet. 1990 Jan;27(1):65-6. doi: 10.1136/jmg.27.1.65.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Female
  • Fetal Diseases
  • Genetic Markers
  • Humans
  • Male
  • Phenylketonurias / diagnosis
  • Phenylketonurias / genetics*
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • Pregnancy
  • Prenatal Diagnosis

Substances

  • Genetic Markers