Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage

This publication has 20 references indexed in Scilit:

• Phenylalanine-hydroxylating system in the human fetus at different developmental ages
  Biochimica et Biophysica Acta (BBA) - General Subjects, 1971
• CHILDREN OF MOTHERS WITH PHENYLKETONURIA
  The Lancet, 1970
• Maternal phenylketonuria: Implications for growth and development
  The Journal of Pediatrics, 1968
• Phenylketonuria. Mass screening of newborns in Ireland.
  Archives of Disease in Childhood, 1968
• A THIRD ALLELE AT THE PHENYLALANINE-HYDROXYLASE LOCUS IN MILD PHENYLKETONURIA (HYPERPHENYLALANEWEMIA)
  The Lancet, 1968
• PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIA
  The Lancet, 1967
• EFFECT OF DIETARY TREATMENT ON FREQUENCY OF PHENYLKETONURIA GENE
  The Lancet, 1967
• The birthplaces of parents and grandparents of a series of patients with phenylketonuria in south-east England
  Annals of Human Genetics, 1961
• On the Roles of Directed and Random Changes in Gene Frequency in the Genetics of Populations
  Evolution, 1948
• PHENYLKETONURIA A PROBLEM IN EUGENICS
  The Lancet, 1946