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：

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

页码：650 / 657

页数：8

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