9号染色体,Chromosome 9
1)Chromosome 99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。
英文短句/例句

1.Study of Microsatellite Replication Error on Chromosome 9 in Acute Leukemia;急性白血病9号染色体微卫星复制错误的研究
2.The analyisis of genetic effects for pericentric inversions of chromosome 9 in 17 case of children.9号染色体臂间倒位17例患儿的遗传效应分析
3.Obtaining and Identification of Chinese Cabbage Alien Addition Lines with Chromosome 3, 6 and 9 of Cabbage;附加甘蓝3号、6号、9号染色体的大白菜异附加系获得与鉴定
4.Loss of Heterozygosity on Chromosome 9 in Esophageal Squamous Cell Carcinoma and Its Precursor Lesion;食管鳞状细胞癌9号染色体等位基因杂合性丢失的研究
5.Loss of Multi-sites Allele Heterozygosity on Chromosome 9 in Esophageal Carcinoma;食管癌9号染色体多位点等位基因杂合性丢失的研究
6.Deletions of Derivative Chromosome 9 in 138 Patients with Chronic Myeloid Leukemia138例慢性髓系白血病衍生9号染色体缺失的研究
7.Refined mapping analysis on candidate regions of tumor suppressor locus on chromosome 9 in gastric cancer9号染色体胃癌抑癌基因候选区域精细定位分析
8.Clinical and Experimental Studies of Derivative Chromosome 9 Deletion in Patients with Ph-positive Leukemia;Ph+染色体白血病患者中衍生9号染色体部分序列缺失的临床和实验研究
9.Comparative Research of the LOH Allelomorphic Gene on Chromosome 9 between Esophageal Squamous Carcinoma and Cervical Squamous Carcinoma食管鳞状细胞癌和宫颈鳞状细胞癌中9号染色体等位基因杂合性缺失的比较研究
10.Loss of Heterozygosity on Chromosome 9 and PTCH1 Expression in Cutaneous Squamous Cell Carcinoma and Basal Cell Carcinoma皮肤鳞状细胞癌与基底细胞癌9号染色体杂合性丢失及PTCH1表达的研究
11.Study on the Loss of Heterozygosity on Chromosome 3,7,8,9,17 in Clear Cell Renal Carcinoma肾透明细胞癌3、7、8、9、17号染色体的杂合性缺失研究
12.The Research on the Application of Fluorescence in Situ Hybridization in Chromosome 9 and 17 in Diagnosis of Urinary Bladder Cancer荧光原位杂交在9、17号染色体诊断膀胱癌中的应用研究
13.Transitional cell carcinoma of urinary bladder related loss of heterozygosity of microsatellite loci on chromosomes 9 and 17 in Chinese国人9号和17号染色体膀胱移行细胞癌相关微卫星位点的杂合性丢失
14.Significance of Monosome 7 or Deletion of the Long Arm of Chromosome 7单体7或7号染色体长臂缺失的意义
15.Microdissection and Microcloning of Swine Chromosome 12;猪12号染色体显微切割与微克隆研究
16.Evolution of the Isochore Structure on Human Chromosome 18;人类18号染色体同质段的进化研究
17.Chromosome 1q amplification and multiple myeloma1号染色体长臂扩增与多发性骨髓瘤
18.Analysis on karyotype of Galega orientalis cv. Xinyin No.1新引1号东方山羊豆染色体核型分析
相关短句/例句

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 8,9,178、9、17号染色体
4)Derivative chromosome 9 deletions衍生9号染色体缺失
5)Human chromosome 9人类第9号染色体
6)corollinae chromosome 9白花甜菜9号染色体
1.We previously analysis BAC microarrays of corollinae chromosome 9 using florescence special expression mRNA of B.先前的研究利用甜菜M14品系和栽培甜菜花期花序mRNA对白花甜菜9号染色体BAC芯片进行杂交,筛选到16-M11和26-L15两个M14甜菜花期特异表达BAC克隆。
延伸阅读

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。