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Annals of the New York Academy of Sciences|January 1, 1985
Genetics and mammalian transport systemsC R Scriver, H S TenenhouseJournal of Inherited Metabolic Disease|July 17, 1999
Genomics, mutations and the Internet: the naming and use of partsC R Scriver, P M NowackiCanadian Journal of Biochemistry|June 1, 1978
The defect in transcellular transport of phosphate in the nephron is located in brush-border membranes in X-linked hypophosphatemia (Hyp mouse model)H S Tenenhouse, C R ScriverJournal of Inherited Metabolic Disease|January 1, 1992
X-linked hypophosphataemia: a homologous phenotype in humans and mice with unusual organ-specific gene dosageC R Scriver, H S TenenhouseClinica Chimica Acta; International Journal of Clinical Chemistry|October 23, 1980
Age-dependent serum sulfate levels in children and adolescentsD E Cole, C R ScriverEndocrinology|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 MohyuddinPageof 18