PRENATAL-DIAGNOSIS OF MENKES DISEASE BY MUTATION ANALYSIS

被引：7

作者：

DAS, S

WHITNEY, S

TAYLOR, J

CHEN, E

LEVINSON, B

VULPE, C

GITSCHIER, J

PACKMAN, S

机构：

[1] UNIV CALIF SAN FRANCISCO,DEPT PEDIAT,DIV GENET,SAN FRANCISCO,CA 94143

[2] UNIV CALIF SAN FRANCISCO,DEPT MED,SAN FRANCISCO,CA 94143

[3] UNIV CALIF SAN FRANCISCO,DEPT BIOCHEM & BIOPHYS,SAN FRANCISCO,CA 94143

[4] UNIV CALIF SAN FRANCISCO,HOWARD HUGHES MED INST,SAN FRANCISCO,CA 94143

[5] CHILDRENS HOSP,MED CTR,DIV MED GENET,OAKLAND,CA 94609

来源：

JOURNAL OF INHERITED METABOLIC DISEASE | 1995年 / 18卷 / 03期

关键词：

D O I：

10.1007/BF00710435

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：364 / 365

页数：2

共 5 条

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[2]

DAS S, 1994, AM J HUM GENET, V55, P883

[3] ISOLATION OF A PARTIAL CANDIDATE GENE FOR MENKES DISEASE BY POSITIONAL CLONING [J].

MERCER, JFB ;

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[4] FIRST TRIMESTER PRENATAL-DIAGNOSIS OF MENKES-DISEASE BY DNA ANALYSIS [J].

TUMER, Z ;

TONNESEN, T ;

BOHMANN, J ;

MARG, W ;

HORN, N .

JOURNAL OF MEDICAL GENETICS, 1994, 31 (08) :615-617

[5] ISOLATION OF A CANDIDATE GENE FOR MENKES DISEASE AND EVIDENCE THAT IT ENCODES A COPPER-TRANSPORTING ATPASE [J].

VULPE, C ;

LEVINSON, B ;

WHITNEY, S ;

PACKMAN, S ;

GITSCHIER, J .

NATURE GENETICS, 1993, 3 (01) :7-13

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