Sequence variation at the phenylalanine hydroxylase gene in the British Isles.Linda Tyfield, Iain Smith, F. Cockburn et al.|PubMed|1997Cited by 22
Comparative multiplex dosage analysis detects whole exon deletions at the phenylalanine hydroxylase locusMary Gable, Linda Tyfield, Margaret M. Williams et al.|Human Mutation|2003Cited by 22
Discordant phenylketonuria phenotypes in one family: the relationship between genotype and clinical outcome is a function of multiple effects.Linda Tyfield, Leanne Hunt, Johannes Zschocke et al.|Journal of Medical Genetics|1995Cited by 15
Mutation analysis of the PKU population in England and Scotland - how and whyLinda Tyfield, Jeff L. Bidwell, A Stephenson|The American Journal of Human Genetics|1994Cited by 0