1) chromosome 16
16号染色体
1.
Objective To localize susceptibility loci in Chinese systemic lupus erythematosus (SLE) cohort by linkage disequilibrium mapping the genomic interval in human chromosome 16 so as to understand whether the pathogenesis of human SLE is related to chromosome 16.
目的 明确 16号染色体与中国人系统性红斑狼疮 (systemic lupus erythematosus,SL E)相关性 ,并对其进行易感基因定位以期发现疾病候选基因。
3) Chromosome 1
1号染色体
1.
Transcriptional Analysis of Chromosome 1 in Diffuse Large B-Cell Lymphoma;
弥漫大B细胞淋巴瘤1号染色体的基因表达分析
2.
Linkage analysis of susceptibility genes for familial schizophrenia on chromosome 1 in Chinese population;
中国人群中家族性精神分裂症与1号染色体的连锁分析
3.
Objective To explore the molecular genetic relationship between chromosome 1 and quantitative trait loci for familial schizophrenia.
目的 探讨家族性精神分裂症的定量性状位点与 1号染色体的分子遗传学关系。
4) 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) Chromosome 7
7号染色体
1.
Analysis of Pericentric Inversion of Chromosome 7 Associated with Turner Syndrome in Family;
7号染色体臂间倒位伴Turner综合征家系分析(英文)
6) chromosome 12
12号染色体
1.
Analysis of allele frequencies of 6 short tandem repeat loci on chromosome 12 in patients with Kashing-Beck disease;
大骨节病患者12号染色体6个STR位点基因频率分析
2.
To analyze the genetic polymorphism of 7 STR loci(D12S1718,D12S1675,D12S358,D12S367,D12S1638,D12S1646 and D12S1682) on chromosome 12 in Shaanxi Hans.
分析了中国汉族人群中12号染色体上7个短串联重复序列(short tandem repeat,STR)基因座的多态性。
3.
Object We carry out a study on microsatellite instability ( MSI) and loss of heterozygosity ( LOH )of the 4 sites linked to TEL gene on chromosome 12, in order to find out the correlation between MSI, LOH of TEL gene and the occurrence, progression of children acute lymphoblastic leukemia ( ALL) .
目的 研究12号染色体TEL基因微卫星不稳定性和杂合性缺失,以探讨其与儿童急性淋巴细胞白血病发生、发展的关系以及检测的临床意义。
补充资料：小体
1.指耳目之类。
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参考词条