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    Article

    DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population

    Thirty-nine Turkish phenylketonuria (PKU) families were investigated for their DNA haplotypes at the phenylalanine hydroxylase (PAH) locus. There was a threefold higher incidence of consanguinity in the popula...

    Uta Lichter-Konecki, Magdalena Schlotter, Canan Yaylak, Meral Özgüç… in Human Genetics (1989)

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    Chapter

    Aminoazidopathien

    Hyperphenylalaninämien (HPA) sind durch persistierende Plasmaphenylalaninkonzentrationen >120 Mmol/1 definiert.

    Kurt Ullrich, Udo Wendel in Monogen bedingte Erbkrankheiten 1 (2000)