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Journal of Inherited Metabolic Disease|January 1, 1981
Urinary pyrimidine excretion in arginase deficiencyE W Naylor, S D CederbaumBiochemical Genetics|April 1, 1976
Glucose 6-phosphate dehydrogenase in rainbow troutS D Cederbaum, A YoshidaBiochimica Et Biophysica Acta|March 28, 1986
Kinetics of inhibition of rat liver and kidney arginases by proline and branched-chain amino acidsN Carvajal, S D CederbaumThe Journal of Pediatrics|January 10, 2001
Laboratory evaluation of urea cycle disordersR D Steiner, S D CederbaumDigestive Diseases and Sciences|December 1, 1980
Gardner's syndrome. Recent developments in research and managementE W Naylor, E LebenthalBiochemical and Biophysical Research Communications|November 13, 1987
Sepiapterin reductase in cultured human cellsJ Ferré, E W NaylorPediatrics|February 1, 1979
Early detection of adenomatous polyposis coli in Gardner's syndromeE W Naylor, E LebenthalPediatrics|February 1, 1978
Newborn screening for maple syrup urine disease (branched-chain ketoaciduria)E W Naylor, R GuthrieClinica Chimica Acta; International Journal of Clinical Chemistry|June 15, 1988
Sepiapterin reductase in human amniotic and skin fibroblasts, chorionic villi, and various blood fractionsJ Ferre, E W NaylorPageof 11