1) derivative chromosome 9
衍生9号染色体
1.
Application of dual-color fluorescence in situ hybridization to study on deletions of derivative chromosome 9 in chronic myelogenous leukemia.;
应用双色荧光原位杂交检测慢性粒细胞白血病衍生9号染色体缺失的研究
2.
To investigate the frequency of derivative chromosome 9 [der(9)] deletions in patients with chronic myelogenous leukemia(CML),karyotype analysis in 138 patients with CML was performed with R-banding technique,and dual fusion fluorescence in situ hybridization(FISH)was used to detect der(9)deletion.
为研究慢性髓系白血病(CML)患者衍生9号染色体[der(9)]部分序列缺失情况,对138例CML患者的骨髓应用R显带技术进行核型分析,并应用bcr-abl1双色双融合DNA探针荧光原位杂交(FISH)检测der(9)部分序列缺失。
3) Chromosome 9
9号染色体
1.
Genetic Effect of Pericentric Inversion of Chromosome 9;
9号染色体臂间倒位的遗传效应研究
2.
Genetic polymorphism of 10 STR loci on chromosome 9 and its forensic application in Chinese population;
中国人群9号染色体10个STR基因座的遗传多态性及其在法医学中的应用
3.
To understand the genetic polymorphism of 10 STR loci on chromosome 9 and reveal the difference on the linkage maps of different populations, the author used a set of nine tetranucleotide ?and one tritranucleotide repeat STR markers on chromosome 9 chosen from Genome Data Bank.
18个无关汉族 3代家系共 131份血样采自甘肃省白银地区 ,常规PCR扩增 9号染色体的 10个STR基因座 ,采用非变性聚丙烯酰胺凝胶电泳分析。
5) derivative chromosome
衍生染色体
1.
Objective To detect the chromosomal origin of supernumerary marker chromosome(SMC) and derivative chromosome which was obliterate in origin.
目的检测来源不明的额外标记染色体和衍生染色体。
6) Human chromosome 9
人类第9号染色体
补充资料：21号染色体部分缺失综合征
21号染色体部分缺失综合征
病名。即21q-综合征。
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