22号染色体,Chromosome 22
1)Chromosome 2222号染色体
1.The relationship between physical distance and genetic distance on chromosome 22;22号染色体遗传距离与物理距离的关系
2.Linkage disequilibrium analysis of chromosome 22 and schizophrenia in a Chinese population;中国人群中精神分裂症与22号染色体的连锁不平衡研究
英文短句/例句
1.Progresses on the genetic study of 22q11 deletion syndrome22号染色体长臂近端微片段缺失综合征的遗传学研究
2.Scanning and Preliminary Functional Analysis of Nasopharyngeal Carcinoma Related Genes on Chromosome 3p21-22;染色体3p21-22区域鼻咽癌相关基因的筛选及其功能的初步研究
3.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
4.Microdissection and Microcloning of Swine Chromosome 12;猪12号染色体显微切割与微克隆研究
5.Evolution of the Isochore Structure on Human Chromosome 18;人类18号染色体同质段的进化研究
6.Chromosome 1q amplification and multiple myeloma1号染色体长臂扩增与多发性骨髓瘤
7.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
8.Prenatal Diagnosis of Ring Chromosome 15.15号环状染色体综合征的产前诊断
9.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%;
10.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。
11.In 22 cases (75. 9% ),there was amyloid in the stroma (asdetermined by Congo Red Staining).22例（75．9％）刚果红染色证实含淀粉样物。
12.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
13.Identification of Double Triplo-3,6 and Acquisition of Primary Triplo-3 and Triplo-6 in Chinese Cabbage大白菜3号、6号染色体双三体及其初级三体的鉴定
14.chromosome elimination染色体丢失，染色体消减
15.chromosome puff染色体胀泡，染色体疏松
16.chromosome mapping染色体作图，染色体定位
17.A chromosome that is not a sex chromosome.常染色体非性染色体的一个常染色体
18.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。
相关短句/例句
the chromosomal translocations of 12,2212、22号染色体异常
3)chromosome 1818号染色体
4)Chromosome 11号染色体
1.Transcriptional Analysis ofChromosome 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 99号染色体
1.Genetic Effect of Pericentric Inversion ofChromosome 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 77号染色体
1.Analysis of Pericentric Inversion ofChromosome 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)
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。
