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R S Wappner

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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

Search research articles

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