POLYMORPHISM OF THE HUMAN COMPLEMENT-C4 AND STEROID 21-HYDROXYLASE GENES - RESTRICTION-FRAGMENT-LENGTH-POLYMORPHISMS REVEALING STRUCTURAL DELETIONS, HOMODUPLICATIONS, AND SIZE VARIANTS

被引：263
|
作者：
SCHNEIDER, PM
CARROLL, MC
ALPER, CA
RITTNER, C
WHITEHEAD, AS
YUNIS, EJ
COLTEN, HR
机构：
[1] CHILDRENS HOSP MED CTR,DIV CELL BIOL,BOSTON,MA 02115
[2] CHILDRENS HOSP MED CTR,DIV IMMUNOL,BOSTON,MA 02115
[3] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,CTR BLOOD RES,BOSTON,MA 02115
[4] HARVARD UNIV,SCH MED,DEPT PEDIAT,BOSTON,MA 02115
[5] HARVARD UNIV,SCH MED,DEPT PATHOL,BOSTON,MA 02115
[6] UNIV MAINZ,INST RECHTSMED,D-6500 MAINZ,FED REP GER
来源：
JOURNAL OF CLINICAL INVESTIGATION | 1986年 / 78卷 / 03期
关键词：
D O I：
10.1172/JCI112623
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：650 / 657
页数：8
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