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W G Ng

Showing results (11-20 of 64) with videos related to

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JAMA|January 9, 1987
Transferase-deficiency galactosemia and the Duarte variantW G Ng, J S Lee, G N Donnell
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1975
Mannitol excretion in galactosemia patientsW G Ng, G N Donnell, W R Bergren
Journal of Inherited Metabolic Disease|January 1, 1978
Prenatal diagnosis and a case report of isovaleric acidaemiaM E Blaskovics, W G Ng, G N Donnell
Journal of Inherited Metabolic Disease|January 1, 1982
Presymptomatic diagnosis: metachromatic leukodystrophy or pseudo arylsulphatase A deficiency?H Kihara, A L Fluharty, W G Ng, et al.
Burns : Journal of the International Society for Burn Injuries|January 18, 2016
Management of the lower gastrointestinal system in burn: A comprehensive reviewJ W G Ng, S A Cairns, C P O'Boyle
Perspectives in Pediatric Pathology|January 1, 1979
Fibroblast culture in the diagnosis of genetic metabolic diseases: comparative histochemical, ultrastructural, and biochemical studiesB H Landing, W G Ng, O Alfi, et al.
The Journal of Pediatrics|July 1, 1989
Milk produced by mothers with galactosemiaW G Ng, Y K Xu, F Kaufman, et al.
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.
Birth Defects Original Article Series|January 1, 1975
Urinary alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
The Journal of Pediatrics|June 1, 1971
Childbearing by a galactosemic womanT F Roe, J G Hallatt, G N Donnell, et al.
Pageof 7

Showing results (11-20 of 64) with videos related to

Sort By:
Pageof 7
JAMA|January 9, 1987
Transferase-deficiency galactosemia and the Duarte variantW G Ng, J S Lee, G N Donnell
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 1, 1975
Mannitol excretion in galactosemia patientsW G Ng, G N Donnell, W R Bergren
Journal of Inherited Metabolic Disease|January 1, 1978
Prenatal diagnosis and a case report of isovaleric acidaemiaM E Blaskovics, W G Ng, G N Donnell
Journal of Inherited Metabolic Disease|January 1, 1982
Presymptomatic diagnosis: metachromatic leukodystrophy or pseudo arylsulphatase A deficiency?H Kihara, A L Fluharty, W G Ng, et al.
Burns : Journal of the International Society for Burn Injuries|January 18, 2016
Management of the lower gastrointestinal system in burn: A comprehensive reviewJ W G Ng, S A Cairns, C P O'Boyle
Perspectives in Pediatric Pathology|January 1, 1979
Fibroblast culture in the diagnosis of genetic metabolic diseases: comparative histochemical, ultrastructural, and biochemical studiesB H Landing, W G Ng, O Alfi, et al.
The Journal of Pediatrics|July 1, 1989
Milk produced by mothers with galactosemiaW G Ng, Y K Xu, F Kaufman, et al.
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.
Birth Defects Original Article Series|January 1, 1975
Urinary alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
The Journal of Pediatrics|June 1, 1971
Childbearing by a galactosemic womanT F Roe, J G Hallatt, G N Donnell, et al.
Pageof 7