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P R Wenham

Showing results (21-30 of 35) with videos related to

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Journal of Clinical Pathology|July 1, 1978
gamma-Glutamyl transferase isoenzymes in human bileP R Wenham, C P Price, H G Sammons
Clinical Chemistry|September 23, 1997
Detecting familial defective apolipoprotein B-100: three molecular scanning methods comparedB G Henderson, P R Wenham, J P Ashby, et al.
Clinical Chemistry|November 1, 1991
Rapid diagnosis of familial defective apolipoprotein B-100 by Amplification Refractory Mutation SystemP R Wenham, C R Newton, R S Houlston, et al.
Annals of Clinical Biochemistry|September 1, 1996
Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and WalesP R Wenham, P Bloomfield, G Blundell, et al.
Lancet (London, England)|September 23, 1989
Genetics of coronary heart diseaseW H Price, S W Morris, A H Kitchin, et al.
Lancet (London, England)|September 8, 1990
Genetic markers of familial coronary heart diseaseW H Price, S W Morris, A H Kitchin, et al.
Atherosclerosis|March 21, 1997
Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UKP R Wenham, B G Henderson, M D Penney, et al.
Lancet (London, England)|June 24, 1989
DNA restriction fragment length polymorphisms as markers of familial coronary heart diseaseW H Price, S W Morris, A H Kitchin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 24, 2002
Apolipoprotein E and neurocognitive outcome from coronary artery surgeryM J A Robson, R P Alston, P J D Andrews, et al.
The European Respiratory Journal|October 1, 1993
Plasma lactate dehydrogenase: a marker of disease activity in cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis?S P Matusiewicz, I J Williamson, P J Sime, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Journal of Clinical Pathology|July 1, 1978
gamma-Glutamyl transferase isoenzymes in human bileP R Wenham, C P Price, H G Sammons
Clinical Chemistry|September 23, 1997
Detecting familial defective apolipoprotein B-100: three molecular scanning methods comparedB G Henderson, P R Wenham, J P Ashby, et al.
Clinical Chemistry|November 1, 1991
Rapid diagnosis of familial defective apolipoprotein B-100 by Amplification Refractory Mutation SystemP R Wenham, C R Newton, R S Houlston, et al.
Annals of Clinical Biochemistry|September 1, 1996
Familial defective apolipoprotein B-100: a study of patients from lipid clinics in Scotland and WalesP R Wenham, P Bloomfield, G Blundell, et al.
Lancet (London, England)|September 23, 1989
Genetics of coronary heart diseaseW H Price, S W Morris, A H Kitchin, et al.
Lancet (London, England)|September 8, 1990
Genetic markers of familial coronary heart diseaseW H Price, S W Morris, A H Kitchin, et al.
Atherosclerosis|March 21, 1997
Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UKP R Wenham, B G Henderson, M D Penney, et al.
Lancet (London, England)|June 24, 1989
DNA restriction fragment length polymorphisms as markers of familial coronary heart diseaseW H Price, S W Morris, A H Kitchin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 24, 2002
Apolipoprotein E and neurocognitive outcome from coronary artery surgeryM J A Robson, R P Alston, P J D Andrews, et al.
The European Respiratory Journal|October 1, 1993
Plasma lactate dehydrogenase: a marker of disease activity in cryptogenic fibrosing alveolitis and extrinsic allergic alveolitis?S P Matusiewicz, I J Williamson, P J Sime, et al.
Pageof 4