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The American Journal of Clinical Nutrition|June 1, 1979
Observations on the composition of milk-substitute products for treatment of inborn errors of amino acid metabolism. Comparisons with human milk. A proposal to rationalize nutrient content of treatment productsR Nayman, M E Thomson, C R Scriver, et al.American Journal of Public Health|December 1, 1982
Prevention of mental retardation in offspring of hyperphenylalaninemic mothersL Cartier, C L Clow, A Lippman-Hand, et al.Genetic Epidemiology|January 1, 1992
Specificity and sensitivity of hexosaminidase assays and DNA analysis for the detection of Tay-Sachs disease gene carriers among Ashkenazic JewsM J Fernandes, F Kaplan, C L Clow, et al.American Journal of Human Genetics|September 1, 1984
Beta-thalassemia disease prevention: genetic medicine appliedC R Scriver, M Bardanis, L Cartier, et al.Journal of Inherited Metabolic Disease|January 1, 1992
Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelinationE Treacy, C L Clow, T R Reade, et al.Journal of Inherited Metabolic Disease|January 1, 1989
Prospective ascertainment of complete and partial serum biotinidase deficiency in the newbornG Dunkel, C R Scriver, C L Clow, et al.The Journal of Pediatrics|March 1, 1985
Ontogeny modifies manifestations of cystinuria genes: implications for counselingC R Scriver, C L Clow, T M Reade, et al.American Journal of Human Genetics|May 1, 1987
The Hartnup phenotype: Mendelian transport disorder, multifactorial diseaseC R Scriver, B Mahon, H L Levy, et al.Ciba Foundation Symposium|June 27, 1979
On being an individual, or: the man in the red hatC R ScriverPageof 18