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Human Genetics|August 1, 1990
Two mutations within the coding sequence of the phenylalanine hydroxylase geneE Svensson, B Andersson, L HagenfeldtJournal of Inherited Metabolic Disease|January 1, 1994
Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotesE Svensson, L Iselius, L HagenfeldtHuman Genetics|May 1, 1991
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria familiesE Svensson, U von Döbeln, L HagenfeldtEuropean Journal of Human Genetics : EJHG|January 1, 1993
Three polymorphisms but no disease-causing mutations in the proximal part of the promoter of the phenylalanine hydroxylase geneE Svensson, Y Wang, R C Eisensmith, et al.Hormone Research|January 1, 1988
Neonatal screening for congenital adrenal hyperplasia using 17-hydroxyprogesterone assay in filter paper blood spotsA Larsson, L Hagenfeldt, U von Döbeln, et al.European Journal of Pediatrics|February 1, 1993
Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patientsE Svensson, U von Döbeln, R C Eisensmith, et al.Journal of Inherited Metabolic Disease|September 5, 1998
Compromised fatty acid oxidation in mitochondrial disordersL HagenfeldtHuman Mutation|January 1, 1992
Two missense mutations causing mild hyperphenylalaninemia associated with DNA haplotype 12E Svensson, R C Eisensmith, B Dworniczak, et al.Acta Paediatrica Scandinavica. Supplement|January 1, 1980
Free fatty acid and ketone body metabolism during exercise in diabetesJ Wahren, L HagenfeldtPageof 129