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W G Ng

Showing results (21-30 of 64) with videos related to

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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.
Molecular Human Reproduction|March 1, 1996
Endometriosis associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)D W Cramer, M D Hornstein, W G Ng, et al.
Molecular Genetics and Metabolism|June 23, 1998
Molecular and biochemical basis of galactosemiaB B Wang, Y K Xu, W G Ng, et al.
Fertility and Sterility|April 1, 1989
Galactose-1-phosphate uridyl transferase activity associated with age at menopause and reproductive historyD W Cramer, B L Harlow, R L Barbieri, et al.
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.
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.
Biochemical Medicine|April 1, 1973
Urinary galactitol in galactosemic patientsT F Roe, W G Ng, W R Bergren, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
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.
Molecular Human Reproduction|March 1, 1996
Endometriosis associated with the N314D mutation of galactose-1-phosphate uridyl transferase (GALT)D W Cramer, M D Hornstein, W G Ng, et al.
Molecular Genetics and Metabolism|June 23, 1998
Molecular and biochemical basis of galactosemiaB B Wang, Y K Xu, W G Ng, et al.
Fertility and Sterility|April 1, 1989
Galactose-1-phosphate uridyl transferase activity associated with age at menopause and reproductive historyD W Cramer, B L Harlow, R L Barbieri, et al.
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.
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.
Biochemical Medicine|April 1, 1973
Urinary galactitol in galactosemic patientsT F Roe, W G Ng, W R Bergren, et al.
Pageof 7