Prenatal diagnosis and carrier detection of classic phenylketonuria by gene analysis

Pediatrics. 1984 Sep;74(3):412-23.
No abstract available

Publication types

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

MeSH terms

  • DNA / genetics
  • Genetic Carrier Screening
  • Humans
  • Pedigree
  • Phenylalanine Hydroxylase / analysis
  • Phenylalanine Hydroxylase / genetics
  • Phenylketonurias / diagnosis*
  • Phenylketonurias / genetics
  • Polymorphism, Genetic
  • Prenatal Diagnosis*

Substances

  • DNA
  • Phenylalanine Hydroxylase