它就是人类第2号染色体。
1号染色体最大，22号染色体最小。
结论9号染色体臂间倒位可导致异常生育。
Conclusion Pericentric inversion of chromosome 9 can result in abnormal fertility.
应用微卫星序列分析16号染色体缺失情况。
To analyze deletion of chromosome 16 by microsatellite analysis.
胶质母细胞瘤9号染色体肿瘤抑制基因的研究。
A study of tumor suppressor genes on chromosome 9 in glioblastomas.
9号染色体上一个常见的等位基因与冠心病有联系。
A Common Allele on Chromosome 9 Associated with Coronary Heart Disease.
除了MHC外，6号染色体上的该区域也包含一组组蛋白基因。
In addition to the MHC, this region on chromosome 6 also contains a cluster of histone genes.
1/5的培养细胞在20号染色体上的特定区域发生突变。
One in five cell-lines mutated a particular region of chromosome 20.
患有WAGR综合症的人缺少11号染色体上的某些基因。
People with WAGR syndrome lack genes that are grouped on chromosome 11.
这些基因是位于15号染色体，其中的23双人类染色体。
These genes are located on chromosome 15, one of the 23 pairs of human chromosomes.
1号染色体最大，与其他染色体相比来说，含有最大数量的基因。
Chromosome 1 is the biggest and contains, per chromosome, the greatest number of genes.
目的分析疑有染色体异常个体的9号染色体异染色质区的变异。
Objective:To analysis the aberration of chromosome 9 heterochromatin for persons suspected to have chromosome abnormalities.
目的探讨7号染色体异常在急性白血病中的发生率及预后意义。
Objective To explore the incidence and prognostic significance of chromosome 7 anomaly in acute leukemia.
2007年，他们的研究论文重点放在了17号染色体上的一个基因上。
Their 2007 paper describes research focused on pinpointing a gene on chromosome 17.
这些蛋白是由位于6号染色体上的一段称为主要组织相溶性复合体基因，MHC编码的。
These proteins are encoded by genes that are grouped on a part of chromosome 6 called the major histocompatibility complex, or MHC.
当前研究中，NIH的研究者分析了33名WAGR综合症患者的11号染色体。
In the current study, the NIH researchers conducted analyses of chromosome 11 in 33 patients with WAGR syndrome.
他们在20号染色体上发现两个新的遗传变异，它们大大增加了男性型秃发的危险。
They found two previously unknown genetic variants on chromosome 20 that substantially increased the risk of male pattern baldness.
2010年人表皮生长因子受体2检测：17号染色体着丝粒拷贝数是否具有影响？
Human Epidermal Growth Factor Receptor 2 Testing in 2010: Does Chromosome 17 Centromere Copy Number Make Any Difference?
这些基因位于人类14号染色体上，它们彼此相邻，科学家已知其中两个与胎儿期间肺部发育相关。
The three genes are located next to each other on human chromosome 14 and two are known to play key roles in fetal lung development.
科学家更深入地推测，这些基因上的益处也许能在那条额外的21号染色体上获得增加。
Scientists have long suspected that such genetic benefits might accrue from having an extra chromosome 21.
根据一项发表在《自然》杂志的研究，这类“瘦身”基因由人类第16号染色体上的28个基因组成。
According to a study published in the journal Nature, the genes in question are a group of 28 that form part of chromosome 16.
1号染色体的排序是来自英国和美国的150名专家历时10年完成的，首次由《自然》杂志在网上公开。
The sequence of chromosome 1, which is published online by the journal Nature, took a team of 150 British and American scientists 10 years to complete.
位于22号染色体的遗传改变我们早已知之，他说，但是引起患病危险升高的确切基因仍不清楚。
The genetic changes on chromosome 22 have been known for some time, he says, but the exact genes that cause the increase in risk still remain unclear.
就此，15号染色体上成为研究热点的这一区域存在另外两种编码尼古丁受体的基因，提示实际情况将更为复杂。
That, and the fact that the region of chromosome 15 under scrutiny has two other nicotine-receptor genes in it, suggests the situation may indeed be more complex.
方法应用原位引物标记(PRINS)在8例女性外周血淋巴细胞培养标本中检测了X、18号染色体。
Methods Chromosomes X, 18 were detected by the primed in situ labeling (PRINS) in eight samples of female peripheral blood cultures.
1995年，在丹麦研究人员发表关于13号染色体的文章之后，第一则关于“尿床的遗传因素”的消息曾引起轰动。
In 1995, the first news of a genetic basis for bed-wetting made headlines, after Danish researchers reported a link to Chromosome 13.
在11号和18号染色体上，我们发现重大的与变异有关的证据。它能帮助说明精神分裂症思维和记忆缺陷。
It also found significant evidence of association with variation on chromosomes 11 and 18 that could help account for the thinking and memory deficits of schizophrenia.
在11号和18号染色体上，我们发现重大的与变异有关的证据。它能帮助说明精神分裂症思维和记忆缺陷。
It also found significant evidence of association with variation on chromosomes 11 and 18 that could help account for the thinking and memory deficits of schizophrenia.
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