Similar articles

• Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia.

  Cohen BE, Szeinberg A, Berman W, Aviad Y, Crispin M, Hirshorn N, Goland R. Cohen BE, et al. Pediatrics. 1969 Nov;44(5):655-60. Pediatrics. 1969. PMID: 5374976 No abstract available.
• Phenylalanine tolerance tests. In families with phenylketonuria and hyperphenylalaninemia.

  Cunningham GC, Day RW, Berman JL, Hsia DY. Cunningham GC, et al. Am J Dis Child. 1969 Jun;117(6):626-35. Am J Dis Child. 1969. PMID: 5771502 No abstract available.
• [Diagnostic and therapeutic problems of phenylketonuria. Parallel study of 2 familial cases as a function of treatment].

  Dhondt JL, Mesmacque-Caby D, Farriaux JP, Fontaine G. Dhondt JL, et al. Lille Med. 1972 Nov;17(10):1432-6. Lille Med. 1972. PMID: 4660861 French. No abstract available.
• Phenylketonuria and its variants.

  Hsia DY. Hsia DY. Prog Med Genet. 1970;7:29-68. Prog Med Genet. 1970. PMID: 4915811 Review. No abstract available.
• Progress in the identification of the heterozygote in phenylketonuria.

  Lehmann WD. Lehmann WD. J Pediatr. 1989 Jun;114(6):915-24. doi: 10.1016/s0022-3476(89)80431-7. J Pediatr. 1989. PMID: 2566668 Review. No abstract available.