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

被引：31
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
收藏
页码：1205 / 1208
页数：4
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