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C R Scriver

Showing results (281-290 of 317) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.
Transactions of the American Neurological Association|January 1, 1973
Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population and identification of a new retardation syndrome with possible linkage to the Tay-Sachs geneE Andermann, F Andermann, G Patry, et al.
American Journal of Human Genetics|September 1, 1984
Beta-thalassemia disease prevention: genetic medicine appliedC R Scriver, M Bardanis, L Cartier, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980
Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"C R Scriver, D E Cole, S A Houghton, et al.
Bone|January 31, 2004
Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp miceZ Q Qiu, R Travers, F Rauch, et al.
Pediatric Neurology|May 1, 1995
Glutaric acidemia type II: neuroimaging and spectroscopy evidence for developmental encephalomyopathyM I Shevell, G Didomenicantonio, M Sylvain, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelinationE Treacy, C L Clow, T R Reade, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prospective ascertainment of complete and partial serum biotinidase deficiency in the newbornG Dunkel, C R Scriver, C L Clow, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
The Gy mutation: another cause of X-linked hypophosphatemia in mouseM F Lyon, C R Scriver, L R Baker, et al.
Clinical and Experimental Dermatology|July 1, 1993
Familial cold urticariaC M Zip, J B Ross, M W Greaves, et al.
Pageof 32

Showing results (281-290 of 317) with videos related to

Sort By:
Pageof 32
Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part III: Impact; a prospective studyJ T Coulombe, B L Kammerer, H L Levy, et al.
Transactions of the American Neurological Association|January 1, 1973
Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population and identification of a new retardation syndrome with possible linkage to the Tay-Sachs geneE Andermann, F Andermann, G Patry, et al.
American Journal of Human Genetics|September 1, 1984
Beta-thalassemia disease prevention: genetic medicine appliedC R Scriver, M Bardanis, L Cartier, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1980
Cord-blood tyrosine levels in the full-term phenylketonuric fetus and the "justification hypothesis"C R Scriver, D E Cole, S A Houghton, et al.
Bone|January 31, 2004
Effect of gene dose and parental origin on bone histomorphometry in X-linked Hyp miceZ Q Qiu, R Travers, F Rauch, et al.
Pediatric Neurology|May 1, 1995
Glutaric acidemia type II: neuroimaging and spectroscopy evidence for developmental encephalomyopathyM I Shevell, G Didomenicantonio, M Sylvain, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Maple syrup urine disease: interrelations between branched-chain amino-, oxo- and hydroxyacids; implications for treatment; associations with CNS dysmyelinationE Treacy, C L Clow, T R Reade, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prospective ascertainment of complete and partial serum biotinidase deficiency in the newbornG Dunkel, C R Scriver, C L Clow, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1986
The Gy mutation: another cause of X-linked hypophosphatemia in mouseM F Lyon, C R Scriver, L R Baker, et al.
Clinical and Experimental Dermatology|July 1, 1993
Familial cold urticariaC M Zip, J B Ross, M W Greaves, et al.
Pageof 32