Showing results (31-40 of 1,285) with videos related to
Sort By:
Pageof 129
Trends in Genetics : TIG|July 3, 1999
Monogenic traits are not simple: lessons from phenylketonuriaC R Scriver, P J WatersThe Journal of Clinical Investigation|March 1, 1975
Orthophosphate transport in the erythrocyte of normal subjects and of patients with X-linked hypophosphatemiaH S Tenenhouse, C R ScriverPediatric Research|January 1, 1982
Cystinotic and normal fibroblasts: differential protection in cystine-free medium by dithiothreitolG A Lancaster, C R ScriverJournal of Chromatography|October 9, 1981
Microassay of inorganic sulfate in biological fluids by controlled flow anion chromatographyD E Cole, C R ScriverJournal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part I: Reconciling retrospective and prospective findingsC R Scriver, H L LevyAnnals 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 ScriverPageof 129