Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)
- 2 September 1967
- Vol. 3 (5565) , 579-581
- https://doi.org/10.1136/bmj.3.5565.579
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
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- Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuriaThe Journal of Pediatrics, 1966
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- Dietary and Biochemical Control of PhenylketonuriaBMJ, 1961
- Further Experiences in the Treatment of PhenylketonuriaBMJ, 1961
- THE EARLY SYMPTOMS OF PHENYLKETONURIAPediatrics, 1961
- AN ENZYMATIC SPECTROPHOTOMETRIC METHOD FOR THE DETERMINATION OF PHENYLALANINE IN BLOOD1960
- Paper Chromatographic Method for Estimation of Phenylalanine.Experimental Biology and Medicine, 1957
- The Phenylalanine Requirement of the Normal InfantJournal of Nutrition, 1955