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C L Clow

Showing results (11-20 of 41) with videos related to

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Canadian 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 Scriver
The American Journal of Clinical Nutrition|July 1, 1971
Plasma amino acids: screening, quantitation, and interpretationC R Scriver, P Lamm, C L Clow
The Journal of Pediatrics|November 1, 1985
So-called thiamin-responsive maple syrup urine disease: 15-year follow-up of the original patientC R Scriver, C L Clow, H George
Clinical Biochemistry|September 1, 1973
On the screening, diagnosis and investigation of hereditary aminoacidopathiesC R Scriver, C L Clow, P Lamm
The New England Journal of Medicine|June 10, 1971
Management of hereditary metabolic disease. The role of allied health personnelC L Clow, T M Reade, C R Scriver
Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R Scriver
The New England Journal of Medicine|November 28, 1974
Advocacy and compliance in genetic screening. Behavior of physicians and clients in a voluntary program of testing for the Tay-Sachs geneE Beck, S Blaichman, C R Scriver, et al.
Journal 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.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Canadian 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 Scriver
The American Journal of Clinical Nutrition|July 1, 1971
Plasma amino acids: screening, quantitation, and interpretationC R Scriver, P Lamm, C L Clow
The Journal of Pediatrics|November 1, 1985
So-called thiamin-responsive maple syrup urine disease: 15-year follow-up of the original patientC R Scriver, C L Clow, H George
Clinical Biochemistry|September 1, 1973
On the screening, diagnosis and investigation of hereditary aminoacidopathiesC R Scriver, C L Clow, P Lamm
The New England Journal of Medicine|June 10, 1971
Management of hereditary metabolic disease. The role of allied health personnelC L Clow, T M Reade, C R Scriver
Pediatrics|December 1, 1981
Outcome of early and long-term management of classical maple syrup urine diseaseC L Clow, T M Reade, C R Scriver
The New England Journal of Medicine|November 28, 1974
Advocacy and compliance in genetic screening. Behavior of physicians and clients in a voluntary program of testing for the Tay-Sachs geneE Beck, S Blaichman, C R Scriver, et al.
Journal 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.
Pageof 5