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Case Reports
. 1966 May;68(5):704-12.
doi: 10.1016/s0022-3476(66)80442-0.

Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria

A J Schneider, S D Garrard
Case Reports

Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria

A J Schneider et al. J Pediatr. 1966 May.
No abstract available

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