1. Atypical phenylketonuric heterozygote. Deficiency in phenylalanine hydroxylase and transaminase activity;Anderson, J.A.; Fisch, R.; Miller, E.; Doeden, D.;Journal of Pediatrics,1966
2. Relation between age, serum phenylalanine level, and phenylpyruvic acid exceretion;Armstrong, M.D.; Low, N.L.;Proceedings of the Society for Experimental Biology and Medicine,1957
3. Phenylalaninemia: a study of the diversity of disorders which produce elevation of blood concentrations of phenylalanine. In Amino Acid Metabolism and Genetic Variation;Auerbach, V.H.; DiGeorge, A.M.; Carpenter, G.G.,1967
4. Isozymes of phenylalanine hydroxylase;Barranger, J.A.; Geiger, P.J.; Huzino, A.; Bessman, S.P.;Science,1972
5. Diagnosis and treatment: interpretation of results of blood screening studies for detection of phenylketonuria;Berry, H.K.; Sutherland, B.S.; Umbarger, B.;Pediatrics,1966