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European Journal of Pediatrics|February 24, 2001
Galactosaemia and allelic variation at the galactose-1-phosphate uridyltransferase gene: a complex relationship between genotype and phenotypeL A TyfieldJournal of Medical Genetics|April 1, 1991
Molecular heterogeneity at the phenylalanine hydroxylase locus in the population of the south-west of EnglandL A Tyfield, M J Osborn, J B HoltonEuropean Journal of Pediatrics|October 1, 1993
Biochemical control, genetic analysis and magnetic resonance imaging in patients with phenylketonuriaJ H Walter, L A Tyfield, J B Holton, et al.Journal of Medical Genetics|August 1, 1989
Identification of the haplotype pattern associated with the mutant PKU allele in the Gypsy population of WalesL A Tyfield, A L Meredith, M J Osborn, et al.European Journal of Pediatrics|March 1, 1991
Persistent hyperthyrotropinaemia since the neonatal period in clinically euthyroid childrenL A Tyfield, S S Abusrewil, S R Jones, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|December 1, 1994
Mutation analysis of the phenylalanine hydroxylase gene using heteroduplex analysis with synthetic DNA constructsL A Tyfield, A Stephenson, J L Bidwell, et al.Journal of Medical Genetics|November 1, 1995
Discordant phenylketonuria phenotypes in one family: the relationship between genotype and clinical outcome is a function of multiple effectsL A Tyfield, J Zschocke, A Stephenson, et al.Journal of Medical Genetics|September 1, 1990
Genetic analysis of treated and untreated phenylketonuria in one familyL A Tyfield, A L Meredith, M J Osborn, et al.American Journal of Human Genetics|February 1, 1997
Sequence variation at the phenylalanine hydroxylase gene in the British IslesL A Tyfield, A Stephenson, F Cockburn, et al.British Journal of Haematology|June 1, 1991
Late onset immune pancytopenia following bone marrow transplantationA Bashey, I Owen, G F Lucas, et al.Pageof 2