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Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1982
Antibodies to distinct polypeptides of RNA polymerase I in sera from patients with rheumatic autoimmune disease
D A Stetler, K M Rose, M E Wenger, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mutation analysis in families with discordant phenotypes of phenylalanine hydroxylase deficiency. Inheritance and expression of the hyperphenylalaninaemias
P Guldberg, H L Levy, R Koch, et al.
Pediatric Research
|
September 1, 1987
Systemic deficiency of the first component of the pyruvate dehydrogenase complex
D S Kerr, L Ho, C M Berlin, et al.
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of 6
Search research articles
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Showing results (51-60 of 53) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 53 results.
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1982
Antibodies to distinct polypeptides of RNA polymerase I in sera from patients with rheumatic autoimmune disease
D A Stetler, K M Rose, M E Wenger, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mutation analysis in families with discordant phenotypes of phenylalanine hydroxylase deficiency. Inheritance and expression of the hyperphenylalaninaemias
P Guldberg, H L Levy, R Koch, et al.
Pediatric Research
|
September 1, 1987
Systemic deficiency of the first component of the pyruvate dehydrogenase complex
D S Kerr, L Ho, C M Berlin, et al.
Page
of 6