PRENATAL-DIAGNOSIS OF ORNITHINE TRANSCARBAMYLASE DEFICIENCY WITH USE OF DNA POLYMORPHISMS

被引：30

作者：

FOX, J

HACK, AM

FENTON, WA

GOLBUS, MS

WINTER, S

KALOUSEK, F

ROZEN, R

BRUSILOW, SW

ROSENBERG, LE

机构：

[1] YALE UNIV,SCH MED,DEPT HUMAN GENET,333 CEDAR ST,POB 3333,NEW HAVEN,CT 06510

[2] UNIV CALIF SAN FRANCISCO,DEPT OBSTET GYNECOL & REPROD SCI,SAN FRANCISCO,CA 94143

[3] MCMASTER UNIV,CTR HUMAN GENET,HAMILTON L8S 4L8,ONTARIO,CANADA

[4] JOHNS HOPKINS UNIV,SCH MED,CHILDRENS MED & SURG CTR,DEPT PEDIAT,BALTIMORE,MD 21205

[5] VALLEY CHILDRENS HOSP,DEPT MED GENET,FRESNO,CA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1986年 / 315卷 / 19期

关键词：

D O I：

10.1056/NEJM198611063151907

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：1205 / 1208

页数：4

共 22 条

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