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C R Scriver

Showing results (191-200 of 317) with videos related to

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Birth Defects Original Article Series|January 1, 1980
The use of cell and organ culture methods to study renal birth defectsM Bergeron, D K Fast, C R Scriver, et al.
Nucleic Acids Research|February 21, 1998
PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databasesP M Nowacki, S Byck, L Prevost, et al.
The New England Journal of Medicine|November 28, 1974
Advocacy and compliance in genetic screening. Behavior of physicians and clients in a voluntary program of testing for the Tay-Sachs geneE Beck, S Blaichman, C R Scriver, et al.
Pediatrics|November 1, 1972
Thiamine-responsive lactice acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liverM G Brunette, E Delvin, B Hazel, et al.
Biochimica Et Biophysica Acta|December 1, 1980
The relationship of 4-aminobutyric acid metabolism to ammoniagenesis in renal cortexP R Goodyer, G Lancaster, M Villeneuve, et al.
Journal of Medical Genetics|July 1, 1993
What young people think and do when the option for cystic fibrosis carrier testing is availableJ Mitchell, C R Scriver, C L Clow, et al.
American Journal of Human Genetics|October 1, 1996
Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schoolsJ J Mitchell, A Capua, C Clow, et al.
Biochimica Et Biophysica Acta|February 28, 1973
A -aminobutyrate pathway in mammalian kidney cortexG Lancaster, F Mohyuddin, C R Scriver, et al.
The New England Journal of Medicine|October 9, 1975
Letter: Plasma-csf glycine ratio in normal and nonketotic hyperglycinemic subjectsC R Scriver, A White, W Sprague, et al.
The Journal of Pediatrics|March 1, 1993
Methylmalonic acidemia with a severe chemical but benign clinical phenotypeE Treacy, C Clow, O A Mamer, et al.
Pageof 32

Showing results (191-200 of 317) with videos related to

Sort By:
Pageof 32
Birth Defects Original Article Series|January 1, 1980
The use of cell and organ culture methods to study renal birth defectsM Bergeron, D K Fast, C R Scriver, et al.
Nucleic Acids Research|February 21, 1998
PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databasesP M Nowacki, S Byck, L Prevost, et al.
The New England Journal of Medicine|November 28, 1974
Advocacy and compliance in genetic screening. Behavior of physicians and clients in a voluntary program of testing for the Tay-Sachs geneE Beck, S Blaichman, C R Scriver, et al.
Pediatrics|November 1, 1972
Thiamine-responsive lactice acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liverM G Brunette, E Delvin, B Hazel, et al.
Biochimica Et Biophysica Acta|December 1, 1980
The relationship of 4-aminobutyric acid metabolism to ammoniagenesis in renal cortexP R Goodyer, G Lancaster, M Villeneuve, et al.
Journal of Medical Genetics|July 1, 1993
What young people think and do when the option for cystic fibrosis carrier testing is availableJ Mitchell, C R Scriver, C L Clow, et al.
American Journal of Human Genetics|October 1, 1996
Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schoolsJ J Mitchell, A Capua, C Clow, et al.
Biochimica Et Biophysica Acta|February 28, 1973
A -aminobutyrate pathway in mammalian kidney cortexG Lancaster, F Mohyuddin, C R Scriver, et al.
The New England Journal of Medicine|October 9, 1975
Letter: Plasma-csf glycine ratio in normal and nonketotic hyperglycinemic subjectsC R Scriver, A White, W Sprague, et al.
The Journal of Pediatrics|March 1, 1993
Methylmalonic acidemia with a severe chemical but benign clinical phenotypeE Treacy, C Clow, O A Mamer, et al.
Pageof 32