Flemming Güttler

A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype

Per Guldberg, Françoise Rey, Johannes Zschocke et al. · The American Journal of Human Genetics · 1998 · 352 citations · Full text

Metabolic Syndrome, Mendelian Disorder, Biochemistry +11

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

Savio L.C. Woo, Alan S. Lidsky, Flemming Güttler et al. · Nature · 1983 · 336 citations

Carrier Detection, Biochemistry, Genetic Disorder +9

Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria

Anthony G. DiLella, Joshua Marvit, Alan S. Lidsky et al. · Nature · 1986 · 247 citations

Specific Dna Haplotype, Genetic Disorder, Genetics +9

Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria

Yoshiyuki Okano, Randy C. Eisensmith, Flemming Güttler et al. · New England Journal of Medicine · 1991 · 237 citations

What do doctors know about statistics?

Henrik R. Wulff, Bjørn Andersen, P. Brandenhoff et al. · Statistics in Medicine · 1987 · 161 citations