1) trisomy 8
8号染色体三体
1.
Clinical and experimental study of 38 cases with trisomy 8;
8号染色体三体38例临床及实验研究
2.
To evaluate the impact of trisomy 8 on cytobiological and clinical features of acute myelomonocytic and monocytic leukemia (M_4, M_5), a total of 56 cases of acute myelomonocytic and monocytic leukemia were investigated.
为了探讨8号染色体三体(8三体)对急性粒单、单核细胞白血病(M4、M5)细胞生物学及临床特征的影响,应用G显带或R显带技术及流式细胞仪对56例M4、M5患者进行核型及免疫表型检测,并对其临床特征进行回顾性分析。
3.
This study was purposed to characterize the first case of acute promyelocitic leukemia (AML-M_3a) with t(15;17) , trisomy 8 and tetrasomy 8,and explore its characteristics of morphology,cytogenetics,molecular biology,immunology and clinical features.
本研究报道首例伴有 8号染色体四体 (四体 8)、8号染色体三体 (三体 8)异常的t(15 ;17)急性早幼粒白血病 (AML M3 a) ,并探讨其形态学、细胞遗传学、分子生物学、免疫学及临床特点。
2) Chromosome 8
8号染色体
1.
Study of Microsatellite Instability and Loss of Heterozygosity on Chromosome 8 in Leukemia;
白血病患者8号染色体微卫星不稳定性和杂合性缺失的研究
2.
Objective: To detect the status of loss of heterozygosity (LOH) on chromosome 8 in prostate carcinoma and high grade prostatic intraepithelial neoplasia (PIN).
目的 :分析原发性前列腺癌及高级别前列腺上皮内肿瘤 (PIN) 8号染色体等位基因杂合性缺失 (LOH)并探讨其意义。
3.
Methods Interphase FISH using Spectrum Red labeled chromosome 8 centromere specific probe was carried out to detect trisomy 8 in 59 cases of ALL and 8 normal controls.
方法 采用荧光素SpectrumRed直接标记 8号染色体着丝粒探针 ,检测了 5 9例ALL病例和 8例正常对照组骨髓细胞 ,并与细胞遗传学 (CG)结果相比较。
3) chromosomes 8p
8号染色体短臂
4) chromosome 8 aberration
8号染色体异常
6) 8 chromosome.
8染色体
补充资料：染色体干涉
染色体干涉
即交叉干涉。区别于染色单体干涉。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条