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Endocrinology|August 1, 1981
Effect of 1,25-dihydroxyvitamin D3 on phosphate homeostasis in the X-linked hypophosphatemic (Hyp) mouseH S Tenenhouse, C R ScriverAmerican Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P HechtmanAmerican Journal of Medical Genetics|June 1, 1985
The effect of Mendelian disease on human health: a measurementT Costa, C R Scriver, B ChildsCanadian Medical Association Journal|September 9, 1972
Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infantP MacLeod, S Mackenzie, C R ScriverThe American Journal of Physiology|February 1, 1983
Hypertaurinuria in the C57BL/6J mouse: altered transport at the renal basolateral membraneR Rozen, C R Scriver, F MohyuddinMolecular Genetics and Metabolism|February 13, 2001
The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patientsT Fukao, C R Scriver, N Kondo, et al.American Journal of Human Genetics|February 1, 1995
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparisonE Treacy, B Childs, C R ScriverAmerican Journal of Medical Genetics|November 1, 1984
Genetic causes of chronic musculoskeletal disease in childhood are commonD Gregory, P Kaplan, C R ScriverHuman Mutation|May 25, 1999
Guidelines and recommendations for content, structure, and deployment of mutation databasesC R Scriver, P M Nowacki, H LehväslaihoCanadian 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 fluxR R McInnes, F Mohyuddin, C R ScriverPageof 129