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1.Recently fluorescence in site hybridization (FISH) techniques has allowed identification of large deletion adjacent to translocation breakpoint on the derivative 9 chromosome [der(9)] in about 10%~15% of Ph+CML and small part of Ph+ALL .
最近,荧光原位杂交(FISH)技术证实约10%~15%的CML患者在衍生9号染色体[der(9)]易位断裂点附近有较大的序列缺失,少数Ph+ALL患者也有der(9)部分序列缺失。 许多研究表明,伴有der(9)部分序列缺失的CML患者有较短的慢性期,较快的疾病进展速度及较短的生存期。收藏指正
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