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G N Donnell

Showing results (51-60 of 73) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1984
Immune functions in methylmalonicaciduriaJ A Church, R Koch, K N Shaw, 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.
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.
Perspectives in Pediatric Pathology|January 1, 1993
Homocystinuria: clinical and pathologic review, with emphasis on thrombotic features, including pulmonary artery thrombosisE R Lieberman, E D Gomperts, K N Shaw, et al.
The New England Journal of Medicine|April 23, 1981
Hypergonadotropic hypogonadism in female patients with galactosemiaF R Kaufman, M D Kogut, G N Donnell, et al.
Pediatrics|August 1, 1991
Verbal dyspraxia in treated galactosemiaC D Nelson, D D Waggoner, G N Donnell, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Journal of Inherited Metabolic Disease|January 1, 1984
Immune functions in methylmalonicaciduriaJ A Church, R Koch, K N Shaw, 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.
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.
Perspectives in Pediatric Pathology|January 1, 1993
Homocystinuria: clinical and pathologic review, with emphasis on thrombotic features, including pulmonary artery thrombosisE R Lieberman, E D Gomperts, K N Shaw, et al.
The New England Journal of Medicine|April 23, 1981
Hypergonadotropic hypogonadism in female patients with galactosemiaF R Kaufman, M D Kogut, G N Donnell, et al.
Pediatrics|August 1, 1991
Verbal dyspraxia in treated galactosemiaC D Nelson, D D Waggoner, G N Donnell, et al.
Pageof 8