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The Journal of Clinical Investigation|December 1, 1983
Metabolism of methylmalonic acid in rats. Is methylmalonyl-coenzyme a racemase deficiency symptomatic in man?J A Montgomery, O A Mamer, C R ScriverNucleic Acids Research|February 21, 1998
PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databasesP M Nowacki, S Byck, L Prevost, et al.Biochimica Et Biophysica Acta|December 1, 1980
The relationship of 4-aminobutyric acid metabolism to ammoniagenesis in renal cortexP R Goodyer, G Lancaster, M Villeneuve, et al.Journal of Medical Genetics|July 1, 1993
What young people think and do when the option for cystic fibrosis carrier testing is availableJ Mitchell, C R Scriver, C L Clow, et al.American Journal of Human Genetics|October 1, 1996
Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schoolsJ J Mitchell, A Capua, C Clow, et al.The Journal of Pediatrics|March 1, 1993
Methylmalonic acidemia with a severe chemical but benign clinical phenotypeE Treacy, C Clow, O A Mamer, et al.Journal of Inherited Metabolic Disease|January 1, 1989
Comparison of ornithine metabolism in hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome, lysinuric protein intolerance and gyrate atrophy fibroblastsJ Botschner, D W Smith, O Simell, et al.Pediatric Research|December 1, 1985
Ornithine loading did not prevent induced hyperammonemia in a patient with hyperornithinemia-hyperammonemia-homocitrullinuria syndromeO Simell, S Mackenzie, C L Clow, et al.American Journal of Medical Genetics|August 1, 1987
Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouseA Boneh, T M Reade, C R Scriver, et al.Metabolism: Clinical and Experimental|September 1, 1985
Normal plasma free amino acid values in adults: the influence of some common physiological variablesC R Scriver, D M Gregory, D Sovetts, et al.Pageof 129