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C R Scriver

Showing results (221-230 of 317) with videos related to

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Lancet (London, England)|April 20, 1974
Is hereditary histidinaemia harmful?J S Popkin, C L Clow, C R Scriver, et al.
American Journal of Medical Genetics|May 1, 1990
Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: paradigm of pitfalls in phenotypesJ J McGill, G Mettler, D S Rosenblatt, 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.
American Journal of Human Genetics|January 1, 1990
Beta-thalassemia genes in French-Canadians: haplotype and mutation analysis of Portneuf chromosomesF Kaplan, G Kokotsis, M DeBraekeleer, et al.
Biochemical and Biophysical Research Communications|May 29, 1981
Intestinal transport of phosphate anion is not impaired in the Hyp (hypophosphatemic) mouseH S Tenenhouse, D K Fast, C R Scriver, 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.
The American Journal of Clinical Nutrition|June 1, 1979
Observations on the composition of milk-substitute products for treatment of inborn errors of amino acid metabolism. Comparisons with human milk. A proposal to rationalize nutrient content of treatment productsR Nayman, M E Thomson, C R Scriver, et al.
American Journal of Human Genetics|August 1, 1994
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutationsR Rozen, A Mascisch, M Lambert, et al.
Oral Surgery, Oral Medicine, and Oral Pathology|September 1, 1988
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseasesS Schwartz, C R Scriver, T M Reade, et al.
Pageof 32

Showing results (221-230 of 317) with videos related to

Sort By:
Pageof 32
Lancet (London, England)|April 20, 1974
Is hereditary histidinaemia harmful?J S Popkin, C L Clow, C R Scriver, et al.
American Journal of Medical Genetics|May 1, 1990
Detection of heterozygotes for recessive alleles. Homocyst(e)inemia: paradigm of pitfalls in phenotypesJ J McGill, G Mettler, D S Rosenblatt, 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.
American Journal of Human Genetics|January 1, 1990
Beta-thalassemia genes in French-Canadians: haplotype and mutation analysis of Portneuf chromosomesF Kaplan, G Kokotsis, M DeBraekeleer, et al.
Biochemical and Biophysical Research Communications|May 29, 1981
Intestinal transport of phosphate anion is not impaired in the Hyp (hypophosphatemic) mouseH S Tenenhouse, D K Fast, C R Scriver, 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.
The American Journal of Clinical Nutrition|June 1, 1979
Observations on the composition of milk-substitute products for treatment of inborn errors of amino acid metabolism. Comparisons with human milk. A proposal to rationalize nutrient content of treatment productsR Nayman, M E Thomson, C R Scriver, et al.
American Journal of Human Genetics|August 1, 1994
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutationsR Rozen, A Mascisch, M Lambert, et al.
Oral Surgery, Oral Medicine, and Oral Pathology|September 1, 1988
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseasesS Schwartz, C R Scriver, T M Reade, et al.
Pageof 32