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              首頁產品中心>FISH探針
              產品搜索:
              16q22/16q23基因缺失探針試劑 (熒光原位雜交法)
              貨號:DF078
              探針名稱:16q22/CEN16,16q23/CEN16
              供貨周期:-
              管理類別:閩廈械備20210090號
              產品概況

              腎臟腫瘤

              Favorable histology Wilmstumor(FHWT)是最為常見的兒童腎臟腫瘤,5年總生存率超過90%。其分子靶標異常與預后、治療方案密切相關(主要來源于 NWTS-5臨床試驗)∶

              ①約15-20%Wilms 瘤伴有WT1(11p13)突變或缺失,與發病、病理分型和遠期預后有關;

              ②1q獲得約占 FHWT的25%,與復發有高相關性,是一新預后指標(AREN11B3試驗);

              ③1p雜合性缺失(LOH)提示預后較差;

              ④16q雜合性缺失(LOH)提示預后較差。

              服務電話
              0592-3300868
              地址:廈門市海滄區山邊洪東路21號3F
              郵箱:sales@diaglogic.com
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