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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.
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.
Metabolism: Clinical and Experimental|September 1, 1985
Normal plasma free amino acid values in adults: the influence of some common physiological variablesC R Scriver, D M Gregory, D Sovetts, et al.
Human Mutation|January 1, 1992
In vitro and in vivo correlations for I65T and M1V mutations at the phenylalanine hydroxylase locusS W John, C R Scriver, R Laframboise, et al.
The Journal of Clinical Investigation|November 1, 1971
Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypesF H Glorieux, C R Scriver, E Delvin, et al.
Canadian Medical Association Journal|May 5, 1973
The frequency of genetic disease and congenital malformation among patients in a pediatric hospitalC R Scriver, J L Neal, R Saginur, et al.
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