Problems in the biochemical detection of heterozygotes for phenylketonuria
- 1 March 1972
- journal article
- Published by Elsevier in Clinical Biochemistry
- Vol. 5 (1-4), 73-81
- https://doi.org/10.1016/s0009-9120(72)80010-9
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- MEASUREMENT OF PHENYLALANINE HYDROXYLASE ACTIVITY IN MAMMALIAN CELLSPublished by Oxford University Press (OUP) ,2009
- Reduction of plasma tyrosine by oral contraceptives and oestrogens: A possible consequence of tyrosine aminotransferase inductionClinica Chimica Acta; International Journal of Clinical Chemistry, 1970
- Technical pitfalls leading to errors in the quantitation of plasma amino acidsClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- A versatile lithium buffer elution system for single column automatic amino acid chromatographyJournal of Chromatography A, 1968
- The effect of progesterone on the concentration of plasma amino acids in manMetabolism, 1967
- Determination of heterozygosity for phenylketonuria on the amino acid analyzerClinica Chimica Acta; International Journal of Clinical Chemistry, 1967
- PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIAThe Lancet, 1967
- Urinary Amino Acids in Pregnancy, Following Progesterone, and Estrogen-ProgesteroneJournal of Clinical Endocrinology & Metabolism, 1967
- A simple test for heterozygosity for phenylketonuriaClinica Chimica Acta; International Journal of Clinical Chemistry, 1967