FIRST TRIMESTER DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE-I

被引：5

作者：

RUMSBY, G ^{[1
]}

UTTLEY, WS ^{[1
]}

KIRK, JM ^{[1
]}

机构：

[1] ROYAL HOSP SICK CHILDREN, EDINBURGH EH9 1LF, MIDLOTHIAN, SCOTLAND

来源：

LANCET | 1994年 / 344卷 / 8928期

关键词：

D O I：

10.1016/S0140-6736(94)91675-6

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1018 / 1018

页数：1

共 5 条

[1] FETAL LIVER ALANINE - GLYOXYLATE AMINOTRANSFERASE AND THE PRENATAL-DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE-1 [J].

DANPURE, CJ ;

JENNINGS, PR ;

PENKETH, RJ ;

WISE, PJ ;

COOPER, PJ ;

RODECK, CH .

PRENATAL DIAGNOSIS, 1989, 9 (04) :271-281

[2] MOLECULAR CHARACTERIZATION AND CLINICAL NSE OF A POLYMORPHIC TANDEM REPEAT IN AN INTRON OF THE HUMAN ALANINE-GLYOXYLATE AMINOTRANSFERASE GENE [J].

DANPURE, CJ ;

BIRDSEY, GM ;

RUMSBY, G ;

LUMB, MJ ;

PURDUE, PE ;

ALLSOP, J .

HUMAN GENETICS, 1994, 94 (01) :55-64

[3]

PURDUE PE, 1991, HUM GENET, V87, P394

[4] CHARACTERIZATION AND CHROMOSOMAL MAPPING OF A GENOMIC CLONE ENCODING HUMAN ALANINE - GLYOXYLATE AMINOTRANSFERASE [J].

PURDUE, PE ;

LUMB, MJ ;

FOX, M ;

GRIFFO, G ;

HAMONBENAIS, C ;

POVEY, S ;

DANPURE, CJ .

GENOMICS, 1991, 10 (01) :34-42

[5]

RUMSBY G, 1992, HUM MOL GENET, V1, P3503

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