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Blood|April 1, 1992
Mutations in Jewish patients with Gaucher diseaseE Beutler, T Gelbart, W Kuhl, et al.Clinical Genetics|August 25, 2004
A previously undescribed frameshift deletion mutation of HFE (c.del277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygoteJ C Barton, C West, P L Lee, et al.Biochemical and Biophysical Research Communications|May 18, 2000
NADH-ferric reductase activity associated with dihydropteridine reductaseP L Lee, C Halloran, A R Cross, et al.Blood Cells, Molecules & Diseases|February 8, 2000
The effect of transferrin polymorphisms on iron metabolismP L Lee, N J Ho, R Olson, et al.Blood Cells, Molecules & Diseases|January 1, 1995
Five new Gaucher disease mutationsE Beutler, T Gelbart, A Demina, et al.Human Genetics|January 1, 1984
Gd (+) Laguna, a new rare glucose-6-phosphate dehydrogenase variant from BrazilT A Weimer, L Schüler, E Beutler, 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.Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the second common Jewish Gaucher disease mutation makes possible population-based screening for the heterozygous stateE Beutler, T Gelbart, W Kuhl, et al.Human Biology|February 1, 1993
Molecular characterization of glucose-6-phosphate dehydrogenase variants from BrazilT A Weimer, F M Salzano, B Westwood, et al.Perceptual and Motor Skills|April 11, 1975
MMPI correlates of extreme field independence and field dependence in a psychiatric populationV Stansell, L E Beutler, C W Neville, et al.Pageof 134