Molecular genetic analysis of phenylketonuria and mental retardation

Res Publ Assoc Res Nerv Ment Dis. 1991:69:193-203.
No abstract available

Publication types

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

MeSH terms

  • Chromosome Deletion
  • Chromosomes, Human, Pair 12
  • Cloning, Molecular*
  • Humans
  • Intellectual Disability / genetics*
  • Phenylalanine Hydroxylase / genetics
  • Phenylketonurias / diagnosis
  • Phenylketonurias / genetics*
  • Polymorphism, Restriction Fragment Length
  • Prenatal Diagnosis

Substances

  • Phenylalanine Hydroxylase