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Acta Paediatrica (Oslo, Norway : 1992)|May 6, 2004
Translating knowledge into practice in the "post-genome" eraC R ScriverBirth Defects Original Article Series|January 1, 1992
Genetic disease: effects on human healthC R ScriverJournal of Inherited Metabolic Disease|January 1, 1996
Genetic screening, testing and treatment: how far can we go?C R ScriverHuman Mutation|December 29, 1999
PAHdb: a locus-specific knowledgebaseC R Scriver, P J Waters, C Sarkissian, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1982
Renal transport of taurine adapts to perturbed taurine homeostasisR Rozen, C R ScriverThe American Journal of Physiology|March 1, 1976
Uptake and metabolism of beta-alanine and L-carnosine by rat tissues in vitro: role in nutritionW Nutzenadel, C R ScriverEuropean Journal of Human Genetics : EJHG|October 22, 1998
Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experienceK C Carter, S Byck, P J Waters, et al.Journal of Bacteriology|November 1, 1970
Neutral amino acid transport in Pseudomonas fluorescensP Hechtman, C R ScriverScience (New York, N.Y.)|March 3, 1972
Loss of a parathyroid hormone-sensitive component of phosphate transport in X-linked hypophosphatemiaF Glorieux, C R ScriverPediatric 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 ScriverPageof 19