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R G Gray

Showing results (61-70 of 101) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1990
A case of the B1 variant of GM2-gangliosidosisR G Gray, A Green, L Rabb, et al.
Prenatal Diagnosis|October 1, 1992
Fumarylacetoacetase activity in cultured and non-cultured chorionic villus cells, and assay in two high-risk pregnanciesM J McCormack, E Walker, R G Gray, et al.
Journal of Adolescent Health Care : Official Publication of the Society for Adolescent Medicine|September 1, 1982
The influence of a family history of CHD risk factors on serum lipoprotein levels in black children and adolescentsR H Durant, C W Linder, S Jay, et al.
Developmental Medicine and Child Neurology|June 30, 2000
Cytochrome oxidase deficiency presenting as birth asphyxiaT A Willis, J Davidson, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Biochemical investigations on a patient with a defect in cytosolic acetoacetyl-CoA thiolase, associated with mental retardationM J Bennett, G P Hosking, M F Smith, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive ethylmalonic-adipic aciduriaA Green, T G Marshall, M J Bennett, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiencyK L Chambliss, R G Gray, G Rylance, et al.
Journal of Medical Genetics|October 1, 1984
A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalitiesR G Gray, G W Lowther, J M Littlewood, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Increased excretion of propan-1,3-diol and 3-hydroxypropionic acid apparently caused by abnormal bacterial metabolism in the gutR J Pollitt, B Fowler, I B Sardharwalla, et al.
Lancet (London, England)|January 14, 1995
Regional variations in medium-chain acyl-CoA dehydrogenase deficiencyH R Seddon, A Green, R G Gray, et al.
Pageof 11

Showing results (61-70 of 101) with videos related to

Sort By:
Pageof 11
Journal of Inherited Metabolic Disease|January 1, 1990
A case of the B1 variant of GM2-gangliosidosisR G Gray, A Green, L Rabb, et al.
Prenatal Diagnosis|October 1, 1992
Fumarylacetoacetase activity in cultured and non-cultured chorionic villus cells, and assay in two high-risk pregnanciesM J McCormack, E Walker, R G Gray, et al.
Journal of Adolescent Health Care : Official Publication of the Society for Adolescent Medicine|September 1, 1982
The influence of a family history of CHD risk factors on serum lipoprotein levels in black children and adolescentsR H Durant, C W Linder, S Jay, et al.
Developmental Medicine and Child Neurology|June 30, 2000
Cytochrome oxidase deficiency presenting as birth asphyxiaT A Willis, J Davidson, R G Gray, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Biochemical investigations on a patient with a defect in cytosolic acetoacetyl-CoA thiolase, associated with mental retardationM J Bennett, G P Hosking, M F Smith, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Riboflavin-responsive ethylmalonic-adipic aciduriaA Green, T G Marshall, M J Bennett, et al.
Journal of Inherited Metabolic Disease|August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiencyK L Chambliss, R G Gray, G Rylance, et al.
Journal of Medical Genetics|October 1, 1984
A case of 2-methylacetoacetyl CoA thiolase deficiency with coincidental chromosome abnormalitiesR G Gray, G W Lowther, J M Littlewood, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 16, 1987
Increased excretion of propan-1,3-diol and 3-hydroxypropionic acid apparently caused by abnormal bacterial metabolism in the gutR J Pollitt, B Fowler, I B Sardharwalla, et al.
Lancet (London, England)|January 14, 1995
Regional variations in medium-chain acyl-CoA dehydrogenase deficiencyH R Seddon, A Green, R G Gray, et al.
Pageof 11