MSH2 genomic deletions are a frequent cause of HNPCC

被引：181

作者：

Wijnen, J

van der Klift, H

Vasen, H

Khan, PM

Menko, F

Tops, C

Heijboer, HM

Lindhout, D

Moller, P

Fodde, R ^{[1
]}

机构：

[1] Leiden Univ, Ctr Med, MGC, Dept Human Genet, Leiden, Netherlands

[2] Leiden Univ, Med Ctr, Dept Gastroenterol, Leiden, Netherlands

[3] Leiden Univ, Med Ctr, Fdn Detect Hereditary Tumors, Leiden, Netherlands

[4] Free Univ Amsterdam Hosp, Dept Clin Genet, Amsterdam, Netherlands

[5] Leiden Univ, Ctr Med, Clin Genet Ctr, Leiden, Netherlands

[6] Erasmus Univ, Dept Clin Genet, MGC, NL-3000 DR Rotterdam, Netherlands

[7] Norwegian Radium Hosp, Oslo, Norway

来源：

NATURE GENETICS | 1998年 / 20卷 / 04期

关键词：

D O I：

10.1038/3795

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：326 / 328

页数：3

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