IDENTIFICATION OF A COMMON MOLECULAR-BASIS FOR COMBINED 17-ALPHA-HYDROXYLASE 17,20-LYASE DEFICIENCY IN 2 MENNONITE FAMILIES

被引：38
作者：
KAGIMOTO, K
WATERMAN, MR
KAGIMOTO, M
FERREIRA, P
SIMPSON, ER
WINTER, JSD
机构：
[1] UNIV TEXAS,SW MED CTR,DEPT BIOCHEM,DEPT OBSTET & GYNECOL,DALLAS,TX 75235
[2] UNIV TEXAS,SW MED CTR,CECIL H & IDA GREEN CTR REPROD BIOL SCI,DALLAS,TX 75235
[3] UNIV ALBERTA,DEPT PEDIAT,EDMONTON T6G 1Z8,ALBERTA,CANADA
[4] UNIV MANITOBA,DEPT PEDIAT,WINNIPEG R3A 1S1,MANITOBA,CANADA
来源：
HUMAN GENETICS | 1989年 / 82卷 / 03期
关键词：
D O I：
10.1007/BF00291172
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：285 / 286
页数：2
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