Constitutional mismatch repair-deficiency syndrome

被引：112

作者：

Wimmer, Katharina ^{[1
]}

Kratz, Christian P. ^{[2
]}

机构：

[1] Med Univ Innsbruck, Dept Med Genet Mol & Clin Pharmacol, Div Human Genet, Innsbruck, Austria

[2] NCI, Clin Genet Branch, Div Canc Epidemiol & Genet, NIH, Rockville, MD 20852 USA

来源：

HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2010年 / 95卷 / 05期

关键词：

EARLY-ONSET; NEUROFIBROMATOSIS TYPE-1; HEMATOLOGICAL MALIGNANCY; MSH6; MUTATIONS; GENE; PREDISPOSES; LEUKEMIA; CANCERS;

D O I：

10.3324/haematol.2009.021626

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：699 / 701

页数：3

共 23 条

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