The genetics of hypoplastic left heart syndrome

被引：29

作者：

Grossfeld, PD

机构：

[1] Univ Calif San Diego, Div Pediat Cardiol, San Diego, CA 92103 USA

[2] Univ Calif San Diego, Dept Med, San Diego, CA 92103 USA

来源：

CARDIOLOGY IN THE YOUNG | 1999年 / 9卷 / 06期

关键词：

D O I：

10.1017/S1047951100005722

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：627 / 632

页数：6

共 43 条

[41] Mutations in the human sterol Δ7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome [J].

Wassif, CA ;

Maslen, C ;

Kachilele-Linjewile, S ;

Lin, D ;

Linck, LM ;

Connor, WE ;

Steiner, RD ;

Porter, FD .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (01) :55-62

[42] HYPOPLASTIC LEFT HEART SYNDROME WITH RHABDOMYOMA OF THE LEFT-VENTRICLE [J].

WATANABE, T ;

HOJO, Y ;

KOZAKI, T ;

NAGASHIMA, M ;

ANDO, M .

PEDIATRIC CARDIOLOGY, 1991, 12 (02) :121-122

[43] Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene [J].

Waterham, HR ;

Wijburg, FA ;

Hennekam, RCM ;

Vreken, P ;

Poll-The, BT ;

Dorland, L ;

Duran, M ;

Jira, PE ;

Smeitink, JAM ;

Wevers, RA ;

Wanders, RJA .

AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) :329-338

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