| 发明名称 |
PROBE FOR DETECTION OF THE FRAGILE X SYNDROME |
| 摘要 |
<p>A nucleic acid fragment capable of hybridising selectively with the human X chromosome at the region Xq27.3 - DXS52 is useful in diagnosing fragile X syndrome and other X-linked disorders.</p> |
| 申请公布号 |
WO9005194(A1) |
申请公布日期 |
1990.05.17 |
| 申请号 |
WO1989GB01303 |
申请日期 |
1989.11.01 |
| 申请人 |
MEDICAL RESEARCH COUNCIL |
发明人 |
DAVIES, KAY, ELIZABETH;BELL, MARTIN;PATTERSON, MARK |
| 分类号 |
G01N33/53;A61K49/00;A61K51/00;C07K14/47;C07K16/18;C12N5/10;C12N15/09;C12P21/08;C12Q1/68;C12R1/91;G01N33/577;G01N33/68 |
主分类号 |
G01N33/53 |
| 代理机构 |
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代理人 |
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| 主权项 |
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| 地址 |
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