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British Journal of Haematology|March 1, 1986
Blood cell phosphogluconolactonase: assay and propertiesE Beutler, W Kuhl, T GelbartThe Journal of Laboratory and Clinical Medicine|April 1, 1975
Placental acid hydrolase purification on concanavalin A-sepharoseE Beutler, E Guinto, W KuhlJournal of Clinical Psychology|February 24, 2001
Antiscientific attitudes: what happens when scientists are unscientific?L E Beutler, T M HarwoodHuman Genetics|August 21, 2001
Large-scale molecular screening for galactosemia alleles in a pan-ethnic populationM Suzuki, C West, E BeutlerBlood|November 1, 1987
Effect of oxalate and malonate on red cell metabolismE Beutler, L Forman, C WestProceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?E Beutler, T Gelbart, A DeminaBlood|June 1, 1981
The effect of alpha-thalassemia on the expression of the beta-thalassemia/HPFH heterozygote in a black familyE Beutler, E Turner, W KuhlAmerican Journal of Human Genetics|May 1, 1990
Linkage of the PvuII polymorphism with the common Jewish mutation for Gaucher diseaseA Zimran, T Gelbart, E BeutlerGenomics|January 1, 1993
Identification of six new Gaucher disease mutationsE Beutler, T Gelbart, C WestThe Journal of Clinical Investigation|January 1, 1986
Erythrocyte glutathione synthetase deficiency leads not only to glutathione but also to glutathione-S-transferase deficiencyE Beutler, T Gelbart, C PegelowPageof 668