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Journal of Inherited Metabolic Disease|January 1, 1983
Histidinaemia. Part II: Impact; a retrospective studyA Rosenmann, C R Scriver, C L Clow, et al.Metabolism: Clinical and Experimental|October 1, 1986
Plasma free amino acid values in normal children and adolescentsD M Gregory, D Sovetts, C L Clow, et al.The American Journal of Clinical Nutrition|June 1, 1979
Observations on the composition of milk-substitute products for treatment of inborn errors of amino acid metabolism. Comparisons with human milk. A proposal to rationalize nutrient content of treatment productsR Nayman, M E Thomson, C R Scriver, et al.American Journal of Human Genetics|August 1, 1994
Mutation profiles of phenylketonuria in Quebec populations: evidence of stratification and novel mutationsR Rozen, A Mascisch, M Lambert, et al.Oral Surgery, Oral Medicine, and Oral Pathology|September 1, 1988
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseasesS Schwartz, C R Scriver, T M Reade, et al.Science (New York, N.Y.)|May 26, 1978
Genetics and Medicine: an evolving relationshipC R Scriver, C Laberge, C L Clow, et al.Human Molecular Genetics|September 1, 1994
Evidence for origin, by recurrent mutation, of the phenylalanine hydroxylase R408W mutation on two haplotypes in European and Quebec populationsS Byck, K Morgan, L Tyfield, et al.Canadian Medical Association Journal|March 24, 2010
A Commentary on Multiple Screening for Aminoacidopathies in the Newborn InfantC R Scriver, C Clow, E Davies, et al.Human Mutation|February 5, 1998
In vitro expression analysis of mutations in phenylalanine hydroxylase: linking genotype to phenotype and structure to functionP J Waters, M A Parniak, P Nowacki, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|August 15, 1983
Apparent gastrointestinal origin of cis-4-hydroxycyclohexanecarboxylic acidJ B Kronick, O A Mamer, J Montgomery, et al.Pageof 129