Classical and mild phenylketonuria in a family.
Open Access
- 1 August 1971
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 46 (248) , 550-552
- https://doi.org/10.1136/adc.46.248.550
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Phenylketonuria: therapeutic problems.BMJ, 1969
- Causes for High Phenylalanine With Normal TyrosineAmerican Journal of Diseases of Children, 1969
- Atypical Phenylketonuria With Borderline or Normal IntelligenceArchives of Pediatrics & Adolescent Medicine, 1968
- PhenylalaninemiaPediatric Clinics of North America, 1968
- Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)BMJ, 1967
- PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIAThe Lancet, 1967