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C R Scriver

Showing results (71-80 of 317) with videos related to

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Pediatric Research|January 1, 1979
Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systemsL Lasley, C R Scriver
The New England Journal of Medicine|December 4, 1980
Phenylketonuria: epitome of human biochemical genetics (first of two parts)C R Scriver, C L Clow
The Johns Hopkins Medical Journal|November 1, 1981
On the heritability of rickets, a common disease (Mendel, mammals and phosphate)C R Scriver, H S Tenenhouse
The New England Journal of Medicine|February 26, 1981
Unexplained serum anion gapD E Cole, C R Scriver
Pediatric Research|January 1, 1984
The effects of Mendelian mutation on renal sulfate and phosphate transport in man and mouseD E Cole, C R Scriver
Pediatrics|January 1, 1977
Knowledge about and attitudes toward genetic screening among high-school students: the Tay-Sachs experienceC L Clow, C R Scriver
Lancet (London, England)|April 7, 1990
Carrier screening for Tay-Sachs diseaseC R Scriver, C L Clow
The International Journal of Biochemistry|May 1, 1992
X-linked hypophosphatemia. A phenotype in search of a causeH S Tenenhouse, C R Scriver
Progress in Clinical and Biological Research|January 1, 1977
Tay-Sachs heterozygote screening: specificity and sensitivityC R Scriver, R J Gold
Pediatric Research|March 1, 1980
Effect of calciotropic hormones and cyclic nucleotides on aminoaciduria and phosphaturiaR R McInnes, C R Scriver
Pageof 32

Showing results (71-80 of 317) with videos related to

Sort By:
Pageof 32
Pediatric Research|January 1, 1979
Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systemsL Lasley, C R Scriver
The New England Journal of Medicine|December 4, 1980
Phenylketonuria: epitome of human biochemical genetics (first of two parts)C R Scriver, C L Clow
The Johns Hopkins Medical Journal|November 1, 1981
On the heritability of rickets, a common disease (Mendel, mammals and phosphate)C R Scriver, H S Tenenhouse
The New England Journal of Medicine|February 26, 1981
Unexplained serum anion gapD E Cole, C R Scriver
Pediatric Research|January 1, 1984
The effects of Mendelian mutation on renal sulfate and phosphate transport in man and mouseD E Cole, C R Scriver
Pediatrics|January 1, 1977
Knowledge about and attitudes toward genetic screening among high-school students: the Tay-Sachs experienceC L Clow, C R Scriver
Lancet (London, England)|April 7, 1990
Carrier screening for Tay-Sachs diseaseC R Scriver, C L Clow
The International Journal of Biochemistry|May 1, 1992
X-linked hypophosphatemia. A phenotype in search of a causeH S Tenenhouse, C R Scriver
Progress in Clinical and Biological Research|January 1, 1977
Tay-Sachs heterozygote screening: specificity and sensitivityC R Scriver, R J Gold
Pediatric Research|March 1, 1980
Effect of calciotropic hormones and cyclic nucleotides on aminoaciduria and phosphaturiaR R McInnes, C R Scriver
Pageof 32