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W G Ng

Showing results (31-40 of 64) with videos related to

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The Journal of Pediatrics|December 1, 1993
Measurements of uridine diphosphate hexoses in galactosemiaW G Ng, Y K Xu, F R Kaufman, et al.
Human Genetics|February 1, 1994
On the molecular nature of the Duarte variant of galactose-1-phosphate uridyl transferase (GALT)H C Lin, L T Kirby, W G Ng, et al.
The Journal of Pediatrics|May 1, 1988
Correlation of ovarian function with galactose-1-phosphate uridyl transferase levels in galactosemiaF R Kaufman, Y K Xu, W G Ng, et al.
Biochemical Medicine|August 1, 1981
Propionate metabolism by cultured skin fibroblasts from normal individuals and patients with methylmalonicaciduria and propionicacidemiaJ Oizumi, T A Giudici, W G Ng, 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.
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.
Biochemical Medicine|April 1, 1976
Study of a family with Los Angeles, Duarte, and classical galactosemia variants of galactose-1-phosphate uridyl transferaseD A Applegarth, G N Donnell, M Mullinger, et al.
Pediatric Neurology|May 1, 1992
Neurologic complications in galactosemiaT K Koch, K A Schmidt, J E Wagstaff, et al.
Pediatrics|March 1, 1974
Galactokinase deficiency in twins: clinical and biochemical studiesN O Olambiwonnu, R McVie, W G Ng, et al.
Cytogenetics and Cell Genetics|January 1, 1977
Duarte variant-galactosemia heterozygote. Repository identification No. GM-1996G N Donnell, W G Ng, O S Alfi, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
The Journal of Pediatrics|December 1, 1993
Measurements of uridine diphosphate hexoses in galactosemiaW G Ng, Y K Xu, F R Kaufman, et al.
Human Genetics|February 1, 1994
On the molecular nature of the Duarte variant of galactose-1-phosphate uridyl transferase (GALT)H C Lin, L T Kirby, W G Ng, et al.
The Journal of Pediatrics|May 1, 1988
Correlation of ovarian function with galactose-1-phosphate uridyl transferase levels in galactosemiaF R Kaufman, Y K Xu, W G Ng, et al.
Biochemical Medicine|August 1, 1981
Propionate metabolism by cultured skin fibroblasts from normal individuals and patients with methylmalonicaciduria and propionicacidemiaJ Oizumi, T A Giudici, W G Ng, 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.
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.
Biochemical Medicine|April 1, 1976
Study of a family with Los Angeles, Duarte, and classical galactosemia variants of galactose-1-phosphate uridyl transferaseD A Applegarth, G N Donnell, M Mullinger, et al.
Pediatric Neurology|May 1, 1992
Neurologic complications in galactosemiaT K Koch, K A Schmidt, J E Wagstaff, et al.
Pediatrics|March 1, 1974
Galactokinase deficiency in twins: clinical and biochemical studiesN O Olambiwonnu, R McVie, W G Ng, et al.
Cytogenetics and Cell Genetics|January 1, 1977
Duarte variant-galactosemia heterozygote. Repository identification No. GM-1996G N Donnell, W G Ng, O S Alfi, et al.
Pageof 7