PHENYLKETONURIA - EPITOME OF HUMAN BIOCHEMICAL GENETICS .2.

被引：83

作者：

SCRIVER, CR

CLOW, CL

机构：

[1] MCGILL UNIV,DEPT BIOL,MONTREAL H3C 3G1,QUEBEC,CANADA

[2] MCGILL UNIV,DEPT PEDIAT,MONTREAL H3C 3G1,QUEBEC,CANADA

[3] MCGILL UNIV,CTR HUMAN GENET,MONTREAL H3C 3G1,QUEBEC,CANADA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1980年 / 303卷 / 24期

关键词：

D O I：

10.1056/NEJM198012113032404

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1394 / 1400

页数：7

共 76 条

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ANDERSEN, AE ;

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[4]

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[5]

BERLOW S, 1980, PEDIATRICS, V65, P837

[6]

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[7] TREATMENT OF CHILDREN WITH PHENYLKETONURIA USING A PHENYLALANINE-FREE PROTEIN HYDROLYSATE (ALBUMAID XP) [J].

BERRY, HK ;

SUTHERLAND, BS ;

HUNT, MM ;

FOGELSON, MH ;

OGRADY, D .

AMERICAN JOURNAL OF CLINICAL NUTRITION, 1976, 29 (04) :351-357

[8]

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[9]

BICKEL H, 1980, NEONATAL SCREENING I

[10]

BICKEL H, 1973, BIBL NUTR DIET, V18, P181

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