Showing results (31-40 of 175) with videos related to
Sort By:
Pageof 18
Pediatric Research|January 1, 1979
Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systemsL Lasley, C R ScriverPediatric Research|January 1, 1984
The effects of Mendelian mutation on renal sulfate and phosphate transport in man and mouseD E Cole, C R ScriverPediatrics|January 1, 1977
Knowledge about and attitudes toward genetic screening among high-school students: the Tay-Sachs experienceC L Clow, C R ScriverThe International Journal of Biochemistry|May 1, 1992
X-linked hypophosphatemia. A phenotype in search of a causeH S Tenenhouse, C R ScriverProgress in Clinical and Biological Research|January 1, 1977
Tay-Sachs heterozygote screening: specificity and sensitivityC R Scriver, R J GoldPediatric Research|March 1, 1980
Effect of calciotropic hormones and cyclic nucleotides on aminoaciduria and phosphaturiaR R McInnes, C R ScriverGenetical Research|October 1, 1990
Conserved loci on the X chromosome confer phosphate homeostasis in mice and humansC R Scriver, H S TenenhouseTrends 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 ScriverPageof 18