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C L Clow

Showing results (21-30 of 41) with videos related to

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Pediatrics|January 1, 1972
A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newbornR McInnes, P Lamm, C L Clow, 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.
Lancet (London, England)|February 13, 1971
Thiamine-responsive maple-syrup-urine diseaseC R Scriver, S Mackenzie, C L Clow, 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.
The New England Journal of Medicine|October 8, 1970
Cystinuria: increased prevalence in patients with mental diseaseC R Scriver, D T Whelan, C L Clow, et al.
Lancet (London, England)|April 20, 1974
Is hereditary histidinaemia harmful?J S Popkin, C L Clow, C R Scriver, 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.
Progress in Medical Genetics|January 1, 1973
On the application of knowledge to the patient with genetic diseaseC L Clow, F C Fraser, C Laberge, 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 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Pediatrics|January 1, 1972
A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newbornR McInnes, P Lamm, C L Clow, 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.
Lancet (London, England)|February 13, 1971
Thiamine-responsive maple-syrup-urine diseaseC R Scriver, S Mackenzie, C L Clow, 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.
The New England Journal of Medicine|October 8, 1970
Cystinuria: increased prevalence in patients with mental diseaseC R Scriver, D T Whelan, C L Clow, et al.
Lancet (London, England)|April 20, 1974
Is hereditary histidinaemia harmful?J S Popkin, C L Clow, C R Scriver, 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.
Progress in Medical Genetics|January 1, 1973
On the application of knowledge to the patient with genetic diseaseC L Clow, F C Fraser, C Laberge, 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 5