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Journal of Inherited Metabolic Disease
|
January 1, 1990
A case of the B1 variant of GM2-gangliosidosis
R 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 pregnancies
M 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 adolescents
R H Durant, C W Linder, S Jay, et al.
Developmental Medicine and Child Neurology
|
June 30, 2000
Cytochrome oxidase deficiency presenting as birth asphyxia
T 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 retardation
M J Bennett, G P Hosking, M F Smith, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Riboflavin-responsive ethylmalonic-adipic aciduria
A Green, T G Marshall, M J Bennett, et al.
Journal of Inherited Metabolic Disease
|
August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency
K 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 abnormalities
R 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 gut
R J Pollitt, B Fowler, I B Sardharwalla, et al.
Lancet (London, England)
|
January 14, 1995
Regional variations in medium-chain acyl-CoA dehydrogenase deficiency
H R Seddon, A Green, R G Gray, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 101) with videos related to
Sort By:
Page
of 11
Journal of Inherited Metabolic Disease
|
January 1, 1990
A case of the B1 variant of GM2-gangliosidosis
R 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 pregnancies
M 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 adolescents
R H Durant, C W Linder, S Jay, et al.
Developmental Medicine and Child Neurology
|
June 30, 2000
Cytochrome oxidase deficiency presenting as birth asphyxia
T 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 retardation
M J Bennett, G P Hosking, M F Smith, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Riboflavin-responsive ethylmalonic-adipic aciduria
A Green, T G Marshall, M J Bennett, et al.
Journal of Inherited Metabolic Disease
|
August 18, 2000
Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency
K 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 abnormalities
R 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 gut
R J Pollitt, B Fowler, I B Sardharwalla, et al.
Lancet (London, England)
|
January 14, 1995
Regional variations in medium-chain acyl-CoA dehydrogenase deficiency
H R Seddon, A Green, R G Gray, et al.
Page
of 11