1号染色体,Chromosome 1
1)Chromosome 11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。
英文短句/例句

1.Chromosome 1q amplification and multiple myeloma1号染色体长臂扩增与多发性骨髓瘤
2.Significance of loss of heterozygosity chromosome 1 in hepatocellular carcinoma肝癌1号染色体等位基因杂合性缺失及临床意义
3.A Primary Screening for Quantitative Trait Loci Affecting Wool Traits in Liangshan Semi-wool Sheep Chromosome 1;凉山半细毛羊1号染色体遗传连锁图和羊毛性状QTL定位研究
4.Mapping a QTL for Backfat on Porcine Chromosome 1 in a Complex Inbred Pig Family;用复杂近交家系定位家猪1号染色体背膘厚QTL的研究
5.Expression of gene MEF2D on amplification district of chromosome 1 in hepatocellular carcinoma1号染色体扩增区MEF2D基因在肝细胞癌组织中的表达
6.Screening the Chromosome Ⅰ Deficiency Stockes by Using Drosophila Pacing-Model利用果蝇心功能衰竭模型筛选1号染色体缺失系
7.Construction and identification of chromosome 1 DNA library of Guangxi Bama miniature swine广西巴马小型猪1号染色体DNA文库的构建和鉴定
8.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
9.The transgenes were localized on chromosome 8, 1, 17 and 2. The results indicated that transgene APP_SWE were integrated stably into the chromosomes of transgenic mice and could be transmitted to offsprings through germ cells.转基因分别整合在 8号、1号、17号和2号染色体上。
10.except for the chromosomes 1 and 14,the female linkage maps of the other chromosomes are longer than the male linkage maps.除了1号和14号染色体以外,其余染色体的雌性连锁图谱的长度均比雄性连锁图谱长。
11.The Packing Coloring and the (p,1) -Total Labelling of Graphs图的泛宽度染色和(p,1)—全标号
12.The Packing Coloring and (p,1)-total Labelling of Some Graphs几类图的泛宽度染色和(p,1)—全标号
13.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
14.Microdissection and Microcloning of Swine Chromosome 12;猪12号染色体显微切割与微克隆研究
15.Evolution of the Isochore Structure on Human Chromosome 18;人类18号染色体同质段的进化研究
16.Prenatal Diagnosis of Ring Chromosome 15.15号环状染色体综合征的产前诊断
17.simultaneous del(13q) and 14q32 rearrangement in 26.1%.13号和14号染色体异常同时存在的检出率为26.1%;
18.The haploid complement consisted of11 metacentrie chromosomes and1 submetacentric chromosome.每一组由11个中部着丝点染色体和1个亚中部着丝点染色体组成。
相关短句/例句

chromosomes 1 and 31和3号染色体
3)amplification district of chromosome 11号染色体扩增区
1.Expression of gene MEF2D on amplification district of chromosome 1 in hepatocellular carcinoma1号染色体扩增区MEF2D基因在肝细胞癌组织中的表达
4)the first chromosome第1染色体
1.Construction of the first chromosome DNA library of ginkgo;银杏第1染色体DNA文库的构建
5)chromosome 1818号染色体
6)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。
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。