Search research articles
Contact Us
Filters
Showing results (121-130 of 317) with videos related to
Page
of 32
Sort By:
American Journal of Human Genetics
|
February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparison
E Treacy, B Childs, C R Scriver
Human Genomics
|
April 6, 2006
Human mutation databases
Richard G H Cotton, C R Scriver
American Journal of Medical Genetics
|
November 1, 1984
Genetic causes of chronic musculoskeletal disease in childhood are common
D Gregory, P Kaplan, C R Scriver
Pediatrics
|
July 1, 1970
Histidinemia discovered by urine screening after renal transplantation
D Rosenblatt, F Mohyuddin, C R Scriver
Human Mutation
|
May 25, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databases
C R Scriver, P M Nowacki, H Lehväslaiho
Canadian Journal of Physiology and Pharmacology
|
May 1, 1980
Tubular reabsorption of alpha-aminoisobutyric acid in the pre-steady-state. Evidence for a cell-to-lumen flux
R R McInnes, F Mohyuddin, C R Scriver
Connective Tissue Research
|
January 1, 1983
Secreted collagen ratios in normal human and osteogenesis imperfecta skin fibroblasts
J Fraser, G A Lancaster, C R Scriver
Human Genetics
|
December 1, 1988
Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytes
D W Smith, C R Scriver, O Simell
Biochimica Et Biophysica Acta
|
December 3, 1971
The ontogeny of amino acid transport in rat kidney. II. Kinetics of uptake and effect of anoxia
K E Baerlocher, C R Scriver, F Mohyuddin
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1975
Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney
C R Scriver, R R McInnes, F Mohyuddin
Page
of 32
Search research articles
Search
Showing results (121-130 of 317) with videos related to
Sort By:
Page
of 32
American Journal of Human Genetics
|
February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparison
E Treacy, B Childs, C R Scriver
Human Genomics
|
April 6, 2006
Human mutation databases
Richard G H Cotton, C R Scriver
American Journal of Medical Genetics
|
November 1, 1984
Genetic causes of chronic musculoskeletal disease in childhood are common
D Gregory, P Kaplan, C R Scriver
Pediatrics
|
July 1, 1970
Histidinemia discovered by urine screening after renal transplantation
D Rosenblatt, F Mohyuddin, C R Scriver
Human Mutation
|
May 25, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databases
C R Scriver, P M Nowacki, H Lehväslaiho
Canadian Journal of Physiology and Pharmacology
|
May 1, 1980
Tubular reabsorption of alpha-aminoisobutyric acid in the pre-steady-state. Evidence for a cell-to-lumen flux
R R McInnes, F Mohyuddin, C R Scriver
Connective Tissue Research
|
January 1, 1983
Secreted collagen ratios in normal human and osteogenesis imperfecta skin fibroblasts
J Fraser, G A Lancaster, C R Scriver
Human Genetics
|
December 1, 1988
Lysinuric protein intolerance mutation is not expressed in the plasma membrane of erythrocytes
D W Smith, C R Scriver, O Simell
Biochimica Et Biophysica Acta
|
December 3, 1971
The ontogeny of amino acid transport in rat kidney. II. Kinetics of uptake and effect of anoxia
K E Baerlocher, C R Scriver, F Mohyuddin
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1975
Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney
C R Scriver, R R McInnes, F Mohyuddin
Page
of 32