RB1 gene mutations in peripheral blood DNA of patients with isolated unilateral retinoblastoma

被引：29

作者：

Klutz, M ^{[1
]}

Horsthemke, B ^{[1
]}

Lohmann, DR ^{[1
]}

机构：

[1] Univ Essen Gesamthsch Klinikum, Inst Humangenet, D-4300 Essen, Germany

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 64卷 / 02期

关键词：

D O I：

10.1086/302254

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：667 / 668

页数：2

共 12 条

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[5] THE REGIONS OF THE RETINOBLASTOMA PROTEIN NEEDED FOR BINDING TO ADENOVIRUS-E1A OR ADENOVIRUS-SV40 LARGE T-ANTIGEN ARE COMMON SITES FOR MUTATIONS
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[8] Incomplete penetrance of familial retinoblastoma linked to germ-line mutations that result in partial loss of RB function
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[9] Frequency of somatic and germ-line mosaicism in retinoblastoma: Implications for genetic counseling
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[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) : 610 - 619
[10] COMPLETE GENOMIC SEQUENCE OF THE HUMAN RETINOBLASTOMA SUSCEPTIBILITY GENE
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