DIAGNOSTIC AND THERAPEUTIC IMPLICATIONS OF PERSISTENT HYPERPHENYLALANINEMIA IN AN INFANT HETEROZYGOUS FOR GENE OF PHENYLKETONURIA

被引：39

作者：

SCHNEIDER, AJ

GARRARD, SD

机构：

来源：

关键词：

D O I：

10.1016/S0022-3476(66)80442-0

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

引用

页码：704 / +

页数：1

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