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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1986
Chromosomal localization of the human apolipoprotein B gene and detection of homologous RNA in monkey intestineS S Deeb, C Disteche, A G Motulsky, et al.Vision Research|May 26, 1999
Analysis of red/green color discrimination in subjects with a single X-linked photopigment geneM A Crognale, D Y Teller, T Yamaguchi, et al.American Journal of Medical Genetics|June 1, 1985
The effect of Mendelian disease on human health: a measurementT Costa, C R Scriver, B ChildsAmerican Journal of Human Genetics|February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparisonE Treacy, B Childs, C R ScriverAnalytical Biochemistry|August 1, 1989
Spectrophotometric assays for the enzymatic hydrolysis of the active metabolites of chlorpyrifos and parathion by plasma paraoxonase/arylesteraseC E Furlong, R J Richter, S L Seidel, et al.American Journal of Human Genetics|March 1, 1984
Paraoxon hydrolysis in human serum mediated by a genetically variable arylesterase and albuminJ Ortigoza-Ferado, R J Richter, S K Hornung, et al.Transplantation Proceedings|July 1, 2008
The impact of conversion from mycophenolate mofetil to mycophenolate sodium among renal transplant recipients on a sirolimus-based regimenB D Kahan, J Podbielski, B ChildsThe Journal of Clinical Investigation|July 1, 1973
Hyperlipidemia in coronary heart disease. 3. Evaluation of lipoprotein phenotypes of 156 genetically defined survivors of myocardial infarctionW R Hazzard, J L Goldstein, M G Schrott, et al.The Journal of Clinical Investigation|July 1, 1973
Hyperlipidemia in coronary heart disease. I. Lipid levels in 500 survivors of myocardial infarctionJ L Goldstein, W R Hazzard, H G Schrott, et al.Pageof 13