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Pediatrics|January 1, 1977
Knowledge about and attitudes toward genetic screening among high-school students: the Tay-Sachs experienceC L Clow, C R ScriverCanadian Medical Association Journal|October 4, 1975
Neonatal hypertyrosinemia and evidence for deficiency of ascorbic acid in Arctic and subarctic peoplesC L Clow, C Laberge, C R ScriverPediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R ScriverJournal 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.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.American Journal of Medical Genetics|August 1, 1984
A private view of heterozygosity: eight-year follow-up study on carriers of the Tay-Sachs gene detected by high school screening in MontrealS Zeesman, C L Clow, L Cartier, 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.Science (New York, N.Y.)|May 26, 1978
Genetics and Medicine: an evolving relationshipC R Scriver, C Laberge, C L Clow, et al.Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part II: Impact; a retrospective studyA Rosenmann, C R Scriver, C L Clow, et al.Metabolism: Clinical and Experimental|October 1, 1986
Plasma free amino acid values in normal children and adolescentsD M Gregory, D Sovetts, C L Clow, et al.Pageof 18