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R S Wappner

Showing results (1-10 of 27) with videos related to

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Pediatric Annals|May 1, 1993
Biochemical diagnosis of genetic diseasesR S Wappner
The Journal of the Indiana State Medical Association|February 1, 1981
Mucopolysaccharide storage disordersR S Wappner
Comprehensive Therapy|April 1, 1987
Update: Lowe's syndromeR S Wappner
The Journal of the Indiana State Medical Association|April 1, 1982
Tay-Sachs carrier detectionR S Wappner
Pediatric Research|June 1, 1976
Hurler syndrome: alpha-L-iduronidase activity in leukocytes as a method for heterozygote detectionR S Wappner, I K Brandt
Journal of Inherited Metabolic Disease|January 1, 1992
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new caseK M Gibson, C F Lee, R S Wappner
Pediatric Research|August 1, 1978
White cell ornithine transcarbamylase activity cannot detect the liver enzyme deficiencyP J Snodgrass, R S Wappner, I K Brandt
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 20, 1975
An artifact in the gas chromatographic analysis of urinary organic acids from phenylketonuric children: decarboxylation of the phenylpyruvic acid during extractionR M Thompson, B G Belanger, R S Wappner, et al.
Human Genetics|July 26, 1977
The Chicago variant of clinical galactosemiaC M Chacko, R S Wappner, I K Brandt, et al.
American Journal of Human Genetics|April 1, 1990
Sequence of the E1 alpha subunit of branched-chain alpha-ketoacid dehydrogenase in two patients with thiamine-responsive maple syrup urine diseaseB Zhang, R S Wappner, I K Brandt, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Pediatric Annals|May 1, 1993
Biochemical diagnosis of genetic diseasesR S Wappner
The Journal of the Indiana State Medical Association|February 1, 1981
Mucopolysaccharide storage disordersR S Wappner
Comprehensive Therapy|April 1, 1987
Update: Lowe's syndromeR S Wappner
The Journal of the Indiana State Medical Association|April 1, 1982
Tay-Sachs carrier detectionR S Wappner
Pediatric Research|June 1, 1976
Hurler syndrome: alpha-L-iduronidase activity in leukocytes as a method for heterozygote detectionR S Wappner, I K Brandt
Journal of Inherited Metabolic Disease|January 1, 1992
3-Methylglutaconyl-coenzyme-A hydratase deficiency: a new caseK M Gibson, C F Lee, R S Wappner
Pediatric Research|August 1, 1978
White cell ornithine transcarbamylase activity cannot detect the liver enzyme deficiencyP J Snodgrass, R S Wappner, I K Brandt
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 20, 1975
An artifact in the gas chromatographic analysis of urinary organic acids from phenylketonuric children: decarboxylation of the phenylpyruvic acid during extractionR M Thompson, B G Belanger, R S Wappner, et al.
Human Genetics|July 26, 1977
The Chicago variant of clinical galactosemiaC M Chacko, R S Wappner, I K Brandt, et al.
American Journal of Human Genetics|April 1, 1990
Sequence of the E1 alpha subunit of branched-chain alpha-ketoacid dehydrogenase in two patients with thiamine-responsive maple syrup urine diseaseB Zhang, R S Wappner, I K Brandt, et al.
Pageof 3