Intelligence quotients and intelligence loss in patients with phenylketonuria and some variant states
- 30 November 1970
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 77 (5), 764-770
- https://doi.org/10.1016/s0022-3476(70)80233-5
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Causes for High Phenylalanine With Normal TyrosineAmerican Journal of Diseases of Children, 1969
- Transient hyperphenylalaninemiaThe Journal of Pediatrics, 1968
- A THIRD ALLELE AT THE PHENYLALANINE-HYDROXYLASE LOCUS IN MILD PHENYLKETONURIA (HYPERPHENYLALANEWEMIA)The Lancet, 1968
- Phenylketonuria 1967Developmental Medicine and Child Neurology, 1967
- Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)BMJ, 1967
- Intelligence in Treated Phenylketonuric Children: A Developmental StudyChild Development, 1966
- Legislation and advances in medical knowledge—acceleration or inhibition?The Journal of Pediatrics, 1966
- Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuriaThe Journal of Pediatrics, 1966
- Atypical phenylketonuric heterozygoteThe Journal of Pediatrics, 1966
- Order of birth, parent-age, and intelligence.Published by American Psychological Association (APA) ,1931