发明名称 NUKLEINSÄURE FRAGMENT DES X-CHROMOSOMEN BEREICHS BETEILIGT AM EMPFINDLICHEN X-SYNDROM, NUKLEOTIDISCHE SONDE UND VERFAHREN FÜR DIE DIAGNOSE VON GEISTIGER ZURÜCKGEBLIEBENHEIT MIT EMPFINDLICHEM X
摘要 <p>A new nucleic acid fragment (I). of at least 156p or nucleotides, is derived from the Xq27-q28 region of the X chromosome. It is contained within the approx. 225 kb DNA segment defined between probes St677 and Do33. Also new are (1) DNA or RNA fragments (Ia) which hybridise selectively with (I); (2) cDNA (Ib) corresponding to (I); (3) probes (II) which hybridise selectively with any of (I),(Ia) and (Ib); (4) fragments of mRNA able to hybridise to (II); (5) recombinant DNA (Ic) contg. at least one fragment (I),(Ia) or (Ib) plus transcription/translation control elements; (6) cloning and expression vectors contg. (Ic); (7) host cell, transformed with these vectors; (8) proteins (III) produced from (Ic) and (9) antibodies (Ab) raised against (III). More specifically (I) is adjacent to, or contains, CpG sites in the region of 20 kb around the 125 kb position as defined on a genetic map.</p>
申请公布号 AT166925(T) 申请公布日期 1998.06.15
申请号 AT19920907135T 申请日期 1992.02.13
申请人 INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) 发明人 MANDEL, JEAN-LOUIS;ROUSSEAU, FRANCOIS;VINCENT, ANNE;HEITZ, DOMINIQUE;OBERLE, ISABELLE
分类号 C12N1/21;C12N15/09;C12N15/12;C12P21/02;C12Q1/68;(IPC1-7):C12Q1/68;C12N15/70;C12N15/79 主分类号 C12N1/21
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