Phenylketonuria: A Reassessment of Mass Infant Screening by Napkin Test
- 2 September 1967
- Vol. 3 (5565) , 582
- https://doi.org/10.1136/bmj.3.5565.582
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)BMJ, 1967
- PHENYLALANINE HYDROXYLASE ACTIVITY IN NEWBORN INFANTSPediatrics, 1964
- PROBLEMS OF ROUTINE SCREENING FOR PHENYLKETONURIAThe Lancet, 1962
- AN ENZYMATIC SPECTROPHOTOMETRIC METHOD FOR THE DETERMINATION OF PHENYLALANINE IN BLOOD1960
- Tests for PhenylketonuriaBMJ, 1959