Molecular genetics of phenylketonuria and its implications.
- 1 November 1989
- journal article
- review article
- Vol. 45 (5) , 667-70
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Population genetics of a diseaseNature, 1987
- Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuriaThe Journal of Pediatrics, 1987
- Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuriaNature, 1986
- PRENATAL DIAGNOSIS OF CLASSIC PHENYLKETONURIA BY DNA ANALYSISThe Lancet, 1985
- Projections of a rebound in frequency of mental retardation from phenylketonuriaApplied Research in Mental Retardation, 1982
- Phenylketonuria: Epitome of Human Biochemical GeneticsNew England Journal of Medicine, 1980
- Maternal Phenylketonuria and HyperphenylalaninemiaNew England Journal of Medicine, 1980
- Intellectual Development and Academic Achievement of Children Treated Early for PhenylketonuriaDevelopmental Medicine and Child Neurology, 1979
- Hyperphenylalaninemia Due to a Deficiency of BiopterinNew England Journal of Medicine, 1978
- NEW VARIANT OF PHENYLKETONURIA WITH PROGRESSIVE NEUROLOGICAL ILLNESS UNRESPONSIVE TO PHENYLALANINE RESTRICTIONThe Lancet, 1975