Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage
- 1 May 1975
- journal article
- Published by Wiley in Annals of Human Genetics
- Vol. 38 (4), 461-469
- https://doi.org/10.1111/j.1469-1809.1975.tb00635.x
Abstract
Click on the article title to read more.Keywords
This publication has 20 references indexed in Scilit:
- Phenylalanine-hydroxylating system in the human fetus at different developmental agesBiochimica et Biophysica Acta (BBA) - General Subjects, 1971
- CHILDREN OF MOTHERS WITH PHENYLKETONURIAThe Lancet, 1970
- Maternal phenylketonuria: Implications for growth and developmentThe 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 HYPERPHENYLALANINÆMIAThe Lancet, 1967
- EFFECT OF DIETARY TREATMENT ON FREQUENCY OF PHENYLKETONURIA GENEThe Lancet, 1967
- The birthplaces of parents and grandparents of a series of patients with phenylketonuria in south-east EnglandAnnals of Human Genetics, 1961
- On the Roles of Directed and Random Changes in Gene Frequency in the Genetics of PopulationsEvolution, 1948
- PHENYLKETONURIA A PROBLEM IN EUGENICSThe Lancet, 1946