PROBE FOR DETECTION OF THE FRAGILE X SYNDROME,申请号GB1989001303-传众专利搜索

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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	WO1990005194(A1)	申请公布日期	1990.05.17
申请号	GB1989001303	申请日期	1989.11.01
申请人		发明人
分类号		主分类号
代理机构		代理人
主权项
地址

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