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The Journal of Biological Chemistry|March 5, 1991
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variantsE Beutler, W Kuhl, T Gelbart, et al.Acta Haematologica|January 13, 2001
Three Gaucher-disease-producing mutations in a patient with Gaucher disease: mechanism and diagnostic implicationsE Beutler, H Liebman, T Gelbart, et al.Clinical Genetics|March 21, 2002
A previously undescribed nonsense mutation of the HFE geneE Beutler, M J Griffin, T Gelbart, et al.Blood|October 9, 1999
The molecular basis of a case of gamma-glutamylcysteine synthetase deficiencyE Beutler, T Gelbart, T Kondo, et al.Acta Haematologica|February 29, 2000
Effect of ozone on red blood cell enzymes and intermediatesA Zimran, G Wasser, L Forman, et al.Blood Cells, Molecules & Diseases|January 1, 1995
A strategy for cloning the hereditary hemochromatosis geneE Beutler, T Gelbart, C West, et al.Blood|April 1, 1992
Mutations in Jewish patients with Gaucher diseaseE Beutler, T Gelbart, W Kuhl, et al.Blood|January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemiaE Beutler, R Moroose, L Kramer, et al.Blood Cells, Molecules & Diseases|January 1, 1995
Five new Gaucher disease mutationsE Beutler, T Gelbart, A Demina, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1985
Heterogeneity in type I Gaucher disease demonstrated by restriction mapping of the geneJ Sorge, T Gelbart, C West, et al.Pageof 42