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C R Scriver

Showing results (201-210 of 317) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|May 31, 1974
The application of an automated hexosaminidase assay to genetic screeningE Delvin, A Pottier, C R Scriver, et al.
Lancet (London, England)|February 13, 1971
Thiamine-responsive maple-syrup-urine diseaseC R Scriver, S Mackenzie, C L Clow, 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.
L'Union Medicale Du Canada|March 1, 1975
[The genetic medicine network in Quebec: An integrated program for diagnosis, counseling and treatment of hereditary metabolic diseases]C Laberge, C R Scriver, C L Clow, 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.
Human Mutation|January 1, 1992
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locusS W John, C R Scriver, R Laframboise, et al.
Human Genetics|October 1, 1987
Hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase. Unusual gene dosage effect in heterozygotesC R Scriver, C L Clow, P Kaplan, et al.
Medical and Pediatric Oncology|January 1, 1989
Neuroblastoma screening: the Canadian experienceB Lemieux, C Auray-Blais, R Giguère, et al.
Pageof 32

Showing results (201-210 of 317) with videos related to

Sort By:
Pageof 32
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 31, 1974
The application of an automated hexosaminidase assay to genetic screeningE Delvin, A Pottier, C R Scriver, et al.
Lancet (London, England)|February 13, 1971
Thiamine-responsive maple-syrup-urine diseaseC R Scriver, S Mackenzie, C L Clow, 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.
L'Union Medicale Du Canada|March 1, 1975
[The genetic medicine network in Quebec: An integrated program for diagnosis, counseling and treatment of hereditary metabolic diseases]C Laberge, C R Scriver, C L Clow, 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.
Human Mutation|January 1, 1992
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locusS W John, C R Scriver, R Laframboise, et al.
Human Genetics|October 1, 1987
Hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase. Unusual gene dosage effect in heterozygotesC R Scriver, C L Clow, P Kaplan, et al.
Medical and Pediatric Oncology|January 1, 1989
Neuroblastoma screening: the Canadian experienceB Lemieux, C Auray-Blais, R Giguère, et al.
Pageof 32