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Lancet (London, England)|March 9, 1985
Prenatal diagnosis of classic phenylketonuria by DNA analysisA S Lidsky, F Güttler, S L WooAmerican Journal of Human Genetics|May 1, 1990
Recurrent mutation in the human phenylalanine hydroxylase geneY Okano, T Wang, R C Eisensmith, et al.Nature|August 3, 1986
Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuriaA G DiLella, J Marvit, A S Lidsky, et al.Nature|November 10, 1983
Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuriaS L Woo, A S Lidsky, F Güttler, et al.European Journal of Pediatrics|March 1, 1991
A prevalent missense mutation in Northern Europe associated with hyperphenylalaninaemiaY Okano, R C Eisensmith, M Dasovich, et al.Lancet (London, England)|February 1, 1986
Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuriaS P Daiger, A S Lidsky, R Chakraborty, et al.Clinical Genetics|November 1, 1989
Impact of medical genetics concerning phenylketonuria: accomplishments, status and practical future possibilitiesF GüttlerThe Biochemical Journal|July 1, 1972
Phospholipid synthesis in HeLa cells exposed to immunoglobulin G and complementF GüttlerThe Journal of Pediatrics|January 1, 1987
Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuriaF Güttler, F D Ledley, A S Lidsky, et al.Human Genetics|May 1, 1987
Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuriaR Chakraborty, A S Lidsky, S P Daiger, et al.Pageof 53