REFERENCES
- Bessman, S.: Discussion. Amer J Dis Child 113:31 (January) 1967.
- Berry, H. K., Sutherland, B. S., Umbarger, B. et al.: Treatment of phenylketonuria. Ibid.,1 pp 2–5.
- Stevenson, R. E. and Huntley, C. C.: Congenital malformations in offspring of phenylketonuric mothers. Pediatrics 40: 33–45 (July) 1967.
- Hsia, D. and O'Flynn, M. E.: Comment. In Gellis, S. S. (Editor): The Year Book of Pediatrics 1969. Chicago, Year Book Medical Publishers, Inc., 1969, p 45.
- Rouse, B. M.: Phenylalanine deficiency syndrome. J Pediat 69: 246–247 (August) 1966.
- Hackney, I. M., Hanley, W. B., Davidson, W. et al.: Phenylketonuria: Mental development, behavior, and termination of low phenylalanine diet. J Pediat 72: 646–655 (May) 1968.
- O'Flynn, M. E. and Hsia, D.: Some observations on the dietary therapy of phenylketonuria. J Pediat 72:260–262 (February) 1968.
- Koch, R., Acosta, P., Fishler, K. et al.: Clinical observations on phenylketonuria. Ibid.,1 pp 6–15.
- Solomons, G., Keleske, L. and Opitz, E.: Evaluation of the effects of terminating the diet in phenylketonuria. J Pediat 69: 596–602 (October) 1966.