COMPOUND HETEROZYGOTES IN HYPERPHENYLALANINEMIA

被引：11

作者：

BARTHOLOME, K

OLEK, K

TREFZ, F

机构：

[1] UNIV BONN,INST HUMAN GENET,D-5300 BONN,FED REP GER

[2] UNIV HEIDELBERG,CHILDRENS HOSP,D-6900 HEIDELBERG,FED REP GER

来源：

HUMAN GENETICS | 1984年 / 65卷 / 04期

关键词：

D O I：

10.1007/BF00291569

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

收藏

页码：405 / 406

页数：2

相关论文

共 6 条

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[2] BLASKOVICS ME, 1971, CALIF MED, V115, P42
[3] KUTTER D, 1979, BR MED J, P797
[4] MATERNAL PHENYLKETONURIA AND HYPERPHENYLALANINEMIA - AN INTERNATIONAL SURVEY OF THE OUTCOME OF UNTREATED AND TREATED PREGNANCIES
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[5] INVIVO RESIDUAL ACTIVITIES OF THE PHENYLALANINE HYDROXYLATING SYSTEM IN PHENYLKETONURIA AND VARIANTS
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[6] SENSITIVE INVIVO ASSAY OF THE PHENYLALANINE HYDROXYLATING SYSTEM WITH A SMALL INTRAVENOUS DOSE OF HEPTADEUTERO L-PHENYLALANINE USING HIGH-PRESSURE LIQUID-CHROMATOGRAPHY AND CAPILLARY GAS CHROMATOGRAPHY-MASS FRAGMENTOGRAPHY
TREFZ, FK
ERLENMAIER, T
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[J]. CLINICA CHIMICA ACTA, 1979, 99 (03) : 211 - 220