1) Human chromosome 9
人类第9号染色体
2) Human chromosome if
人第11号染色体
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。
4) Human chromosome 11
人类11号染色体
5) 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。
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