7 results on '"Trefz, F.K."'
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2. The challenges of managing coexistent disorders with phenylketonuria: 30 cases
3. Propionazidämie und Schallempfindungsschwerhörigkeit: Gibt es eine molekulargenetische Basis?
4. Propionazidämie und Schallempfindungsschwerhörigkeit.
5. Maternal mild hyperphenylalaninaemia: an international survey of offspring outcome
6. 3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects
7. Electroencephalographic evaluation of chronic aspartame ingestion in phenylketonuric heterozygotes (PKUH)
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