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American Journal of Human Genetics|January 1, 1976
Biochemical and genetic studies of plasma and leukocyte alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
Science (New York, N.Y.)|May 12, 1972
Galactonic Acid in galactosemia: identification in the urineW R Bergren, W G Ng, G N Donnell, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 1, 1977
Prenatal diagnosis of galactosemiaW G Ng, G N Donnell, W R Bergren, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Pyruvate carboxylase defect: metabolic studies on cultured skin fibroblastsJ Oizumi, W G Ng, G N Donnell
American Journal of Diseases of Children (1960)|January 1, 1985
Beta-glucuronidase deficiency. A heterogeneous mucopolysaccharidosisJ E Lee, R E Falk, W G Ng, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Deficit of uridine diphosphate galactose in galactosaemiaW G Ng, Y K Xu, F R Kaufman, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 31, 1995
Radiochemical assay of minute quantities of galactose-1-phosphate uridyltransferase activity in erythrocytes and leukocytes of galactosemia patientsY K Xu, F R Kaufman, G N Donnell, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Uridine nucleotide sugars in erythrocytes of patients with galactokinase deficiencyY K Xu, W G Ng, F R Kaufman, et al.
Journal of Inherited Metabolic Disease|January 1, 1978
Biochemical studies of a human low-activity galactose-1-phosphate uridyl transferase variantW G Ng, F Kline, J Lin, et al.
Cytogenetics and Cell Genetics|January 1, 1979
Regional mapping of the gene for human UDPGal 4-epimerase on chromosome 1 in mouse-human hybridsM S Lin, J Oizumi, W G Ng, et al.
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