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1)  chromosome 2
2号染色体
1.
Genetic polymorphism analysis of 8 short tandem repeat loci on chromosome 2 in Chinese Han population in Shaanxi Province;
陕西省汉族人群2号染色体8个STR基因座的遗传多态性研究
2.
A Search for Susceptibility Loci to Essential Hypertension on Chromosome 2 in Hypertensive Patients in Shandong Province
山东省原发性高血压2号染色体基因扫描研究
3.
This thesis aims to find whether there is change in Marek s s-tumor-related host genome by scanning MSI of chicken s chromosome 2 partially, and to provide basic data for biology of formation and development of Marek s s tumor, genetics in anti-disease breeding, and molecule diagnosis in terms of host genome.
通过对鸡2号染色体上部分微卫星不稳定性进行研究,旨在发现是否存在与马立克肿瘤发生相关的宿主基因组改变,为从宿主的角度研究鸡马立克肿瘤发生和发展的生物学、抗病育种的遗传学、分子诊断等方面提供基础资料。
2)  2Ai-2 chromosome
2Ai-2染色体
1.
The populations were detected using EST-PCR markers specific to 2Ai-2 chromosome and genomic in situ hybridization (GISH) in order to study the transmission ratio, types of structure variation as well as pairing behaviour affected by gene Ph1.
中间偃麦草2Ai-2染色体携带抗中国流行的大麦黄矮病GPV和GAV病毒株系的抗病基因。
3)  chromosome 18
18号染色体
4)  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。
5)  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。
6)  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)
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。
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