PRENATAL EXCLUSION OF SEVERE FACTOR-VII DEFICIENCY BY DNA SEQUENCING

被引：17

作者：

MILLAR, DS

COOPER, DN

KAKKAR, VV

SCHWARTZ, M

SCHEIBEL, E

机构：

[1] SECT CLIN GENET,COPENHAGEN,DENMARK

[2] HAEMOPHILIA CTR,COPENHAGEN,DENMARK

来源：

LANCET | 1992年 / 339卷 / 8805期

关键词：

D O I：

10.1016/0140-6736(92)92005-Z

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1359 / 1359

页数：1

共 6 条

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[2]

GRUNDY CB, 1991, BLOOD, V78, P1027

[3]

OBRIEN DP, 1991, BLOOD, V78, P132

[4] THE HUMAN FACTOR-VII GENE IS POLYMORPHIC DUE TO VARIATION IN REPEAT COPY NUMBER IN A MINISATELLITE [J].

OHARA, PJ ;

GRANT, FJ .

GENE, 1988, 66 (01) :147-158

[5] NUCLEOTIDE-SEQUENCE OF THE GENE CODING FOR HUMAN FACTOR-VII, A VITAMIN-K-DEPENDENT PROTEIN PARTICIPATING IN BLOOD-COAGULATION [J].

OHARA, PJ ;

GRANT, FJ ;

HALDEMAN, BA ;

GRAY, CL ;

INSLEY, MY ;

HAGEN, FS ;

MURRAY, MJ .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) :5158-5162

[6]

TRIPLETT DA, 1985, BLOOD, V66, P1284

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