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C R Scriver

Showing results (111-120 of 317) with videos related to

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American Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P Hechtman
American Journal of Medical Genetics|June 1, 1985
The effect of Mendelian disease on human health: a measurementT Costa, C R Scriver, B Childs
Pediatrics|June 1, 1972
Serum parathyroid hormone levels in acquired vitamin D deficiency of infancyC Arnaud, F Glorieux, C R Scriver
Canadian Medical Association Journal|September 9, 1972
Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infantP MacLeod, S Mackenzie, C R Scriver
American Journal of Human Genetics|July 1, 1991
Cystic fibrosis carrier screening by DNA analysis: a pilot study of attitudes among participantsF Kaplan, C Clow, C R Scriver
Lancet (London, England)|October 3, 1970
Toxicity of dithiothreitolH Goldman, C R Scriver, K Aaron
L'Union Medicale Du Canada|August 1, 1985
[Hereditary tyrosinemia and vitamin-dependent rickets in Saguenay. A genetic and demographic approach]G Bouchard, C Laberge, C R Scriver
The American Journal of Physiology|February 1, 1983
Hypertaurinuria in the C57BL/6J mouse: altered transport at the renal basolateral membraneR Rozen, C R Scriver, F Mohyuddin
European Journal of Population = Revue Europeenne De Demographie|September 1, 1988
[Demographic reproduction and genetic transmission in the north-east of the province of Quebec (18th-20th centuries)]G Bouchard, C Laberge, C R Scriver
Molecular Genetics and Metabolism|February 13, 2001
The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patientsT Fukao, C R Scriver, N Kondo, et al.
Pageof 32

Showing results (111-120 of 317) with videos related to

Sort By:
Pageof 32
American Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P Hechtman
American Journal of Medical Genetics|June 1, 1985
The effect of Mendelian disease on human health: a measurementT Costa, C R Scriver, B Childs
Pediatrics|June 1, 1972
Serum parathyroid hormone levels in acquired vitamin D deficiency of infancyC Arnaud, F Glorieux, C R Scriver
Canadian Medical Association Journal|September 9, 1972
Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infantP MacLeod, S Mackenzie, C R Scriver
American Journal of Human Genetics|July 1, 1991
Cystic fibrosis carrier screening by DNA analysis: a pilot study of attitudes among participantsF Kaplan, C Clow, C R Scriver
Lancet (London, England)|October 3, 1970
Toxicity of dithiothreitolH Goldman, C R Scriver, K Aaron
L'Union Medicale Du Canada|August 1, 1985
[Hereditary tyrosinemia and vitamin-dependent rickets in Saguenay. A genetic and demographic approach]G Bouchard, C Laberge, C R Scriver
The American Journal of Physiology|February 1, 1983
Hypertaurinuria in the C57BL/6J mouse: altered transport at the renal basolateral membraneR Rozen, C R Scriver, F Mohyuddin
European Journal of Population = Revue Europeenne De Demographie|September 1, 1988
[Demographic reproduction and genetic transmission in the north-east of the province of Quebec (18th-20th centuries)]G Bouchard, C Laberge, C R Scriver
Molecular Genetics and Metabolism|February 13, 2001
The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patientsT Fukao, C R Scriver, N Kondo, et al.
Pageof 32