| 发明名称 |
Genetic variants on CHR16 as markers for use in breast cancer risk assessment, diagnosis, prognosis and treatment |
| 摘要 |
<p>The invention pertains to certain genetic variants on Chr16q12 as susceptibility variants of breast cancer, in particular the marker rs3803662 and markers in linkage disequilibrium therewith. Methods of risk assessment and diagnosis of increased and/or decreased susceptibility to breast cancer, using such variants are described. The invention further relates to kits for diagnosing a susceptibility to breast cancer.</p> |
| 申请公布号 |
EP2540840(A2) |
申请公布日期 |
2013.01.02 |
| 申请号 |
EP20120153875 |
申请日期 |
2008.03.26 |
| 申请人 |
DECODE GENETICS EHF. |
发明人 |
SULEM, PATRICK;MANOLESCU, ANDREI;STACEY, SIMON |
| 分类号 |
C12Q1/68 |
主分类号 |
C12Q1/68 |
| 代理机构 |
|
代理人 |
|
| 主权项 |
|
| 地址 |
|
