2) trisomy18
18号染色体三体
3) isodicentric chromosome 18
18等臂双着丝粒染色体
1.
Experimental study of whole genomic copy number variations in a fetus with a de novo isodicentric chromosome 18 by array-based comparative genomic hybridization
微阵列比较基因组杂交分析18等臂双着丝粒染色体胎儿全基因组拷贝数变化
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。
参考词条