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Journal of the American Dietetic Association|October 1, 1985
Phenylketonuria, adolescence, and dietM M Hunt, H K Berry, P P White
Journal of Inherited Metabolic Disease|January 1, 1987
Phenylketonuria revisited: treatment of adults with behavioural manifestationsR L Brunner, E H Brown, H K Berry
Clinical Genetics|February 1, 1978
Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygoteC H Wharton, H K Berry, M K Bofinger
Neuroscience and Biobehavioral Reviews|January 1, 1981
Progress in experimental phenylketonuria: a critical reviewC V Vorhees, R E Butcher, H K Berry
Biology of the Neonate|January 1, 1975
Serum amino acid concentrations during pregnancy of women heterozygous for phenylketonuriaH K Berry, I B Poncet, B S Sutherland, et al.
American Journal of Diseases of Children (1960)|October 1, 1980
Elevated meconium lactase activity. Its use as a screening test for cystic fibrosisH K Berry, F W Kellogg, S R Lichstein, et al.
American Journal of Diseases of Children (1960)|February 1, 1982
Diagnosis of phenylalanine hydroxylase deficiency (phenylketonuria)H K Berry, M H Hsieh, M K Bofinger, et al.
Journal of Chromatography|January 11, 1985
Rapid gas chromatographic--mass spectrometric quantitation of gamma-aminobutyric acid in biological specimensE J Norman, E L Wee, H K Berry, et al.
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