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Blood
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October 9, 1999
The molecular basis of a case of gamma-glutamylcysteine synthetase deficiency
E Beutler, T Gelbart, T Kondo, et al.
Acta Haematologica
|
February 29, 2000
Effect of ozone on red blood cell enzymes and intermediates
A Zimran, G Wasser, L Forman, et al.
Blood Cells, Molecules & Diseases
|
January 1, 1995
A strategy for cloning the hereditary hemochromatosis gene
E Beutler, T Gelbart, C West, et al.
Blood
|
April 1, 1992
Mutations in Jewish patients with Gaucher disease
E Beutler, T Gelbart, W Kuhl, et al.
Blood Cells, Molecules & Diseases
|
February 8, 2000
Commentary on HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. Adams
E Beutler, V J Felitti, N J Ho, et al.
Blood
|
January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemia
E Beutler, R Moroose, L Kramer, et al.
Blood Cells, Molecules & Diseases
|
January 1, 1995
Five new Gaucher disease mutations
E 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 gene
J 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 state
E Beutler, T Gelbart, W Kuhl, et al.
Blood
|
December 1, 1980
In vivo survival studies of 51Cr-labeled methyl acetimidate treated erythrocytes in patients with sickle cell disease
T G Gabuzda, T L Chao, M R Berenfeld, et al.
Page
of 9
Search research articles
Search
Showing results (41-50 of 81) with videos related to
Sort By:
Page
of 9
Blood
|
October 9, 1999
The molecular basis of a case of gamma-glutamylcysteine synthetase deficiency
E Beutler, T Gelbart, T Kondo, et al.
Acta Haematologica
|
February 29, 2000
Effect of ozone on red blood cell enzymes and intermediates
A Zimran, G Wasser, L Forman, et al.
Blood Cells, Molecules & Diseases
|
January 1, 1995
A strategy for cloning the hereditary hemochromatosis gene
E Beutler, T Gelbart, C West, et al.
Blood
|
April 1, 1992
Mutations in Jewish patients with Gaucher disease
E Beutler, T Gelbart, W Kuhl, et al.
Blood Cells, Molecules & Diseases
|
February 8, 2000
Commentary on HFE S65C variant is not associated with increased transferrin saturation in voluntary blood donors by Naveen Arya, Subrata Chakrabrati, Robert A. Hegele, Paul C. Adams
E Beutler, V J Felitti, N J Ho, et al.
Blood
|
January 1, 1990
Gamma-glutamylcysteine synthetase deficiency and hemolytic anemia
E Beutler, R Moroose, L Kramer, et al.
Blood Cells, Molecules & Diseases
|
January 1, 1995
Five new Gaucher disease mutations
E 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 gene
J 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 state
E Beutler, T Gelbart, W Kuhl, et al.
Blood
|
December 1, 1980
In vivo survival studies of 51Cr-labeled methyl acetimidate treated erythrocytes in patients with sickle cell disease
T G Gabuzda, T L Chao, M R Berenfeld, et al.
Page
of 9