染色体基因

The supposition is that the cancer may be caused by loss of suppressor genes on these chromosomes.

假设是，癌症可能造成的损失，抑制基因对这些染色体。

Methods Peripheral blood samples were collected from the members in a family with autosomal dominant congenital sutural cataract.

目的 对我国一常染色体显性先天性缝合状白内障家系进行致病基因的定位。

The gene responsible for congenital sutural cataract in a Chinese pedigree is located at chromosome 3q21.1-q26.2 within a 38.6 cM region.

先天性缝合状白内障家系的致病基因位于3号染色体3q21.1-q26.2约38.6 cM区域内。

One of the genes controlling sweat gland in human is located on X chromosome.

控制人类汗腺的一个基因位於X染色体上。

Disruption of Sun1 in mice prevents telomere attachment to the nuclear envelope, efficient homologue pairing and synapsis formation in meiosis.

小鼠中Sun1基因的剔除破坏了减数分裂时期端粒的核膜附着，阻碍了同源染色体配对和联会的形成。

Generally speaking, most causes the blood disease which the skin hemorrhage, the menstruation increase, through inspections and so on routine blood test, marrow may be clear about the diagnosis basically, but to minority difficult case, then must through the special examination method, like the chromosome inspection, the gene order analysis, the blood platelet accumulation function determination be able to diagnose (my branch to apply the above method to diagnose rare May-Hegglin successively recently exceptionally with heredity telangiectasis sickness pedigree each example).

一般而言，多数导致皮肤出血、月经增多的血液疾病，通过血常规、骨髓等检查可基本明确诊断，但对少数疑难病例，则需通过特殊的检测方法，如染色体检查、基因序列分析、血小板聚集功能测定才能确诊（最近我科应用上述方法先后诊断了罕见的May－Hegglin异常和遗传性毛细血管扩张症家系各一例）。

For SSR, maize has 88% of the gene diversity and 76% of the number of alleles found in teosinte Vigouroux et al.

玉米驯化养殖过程中的基因瓶颈以及种植者不断地选择被认为导致了玉米整个染色体组以及标记序列内多样性的下降。

Primary torsion dystonia is a group of movement disorders in which dystonia is the only neurologic characteristic. Dystonias differ in their genetic causes, but the majority show autosomal dominant inheritance.

原发性扭转性肌张力障碍是一组动作障碍，此类肌张力障碍是唯一有神经特徵的，它们的基因原因不同，但是大多数肌张力障碍显示体染色体显性遗传。

And we checked the Y chromosome of tufted deer associate with gene localization by our lab.

结合本实验室的基因定位研究对毛冠鹿的Y染色体进行了验证。

Objective: To illuminate the molecular mechanism and provide basic data and methods for early diagnosis, prevention and treatment of NTDs, studies were made on histopathology, ultramicroscopic pathology, cytogenetics, gene expression of molecular genetics and intervention experiment through maternal folic acid supplyment.

目的 研究NTDs胎儿组织病理学和超微病理学改变、细胞遗传学的染色体改变及分子遗传学的基因表达改变，通过增补叶酸干预实验，为探讨NTDs的分子发病机制、对NTDs的早期诊断和防治提供基础资料和方法。

She gently rebuff ed him, but agreed that they could be friends

她婉言拒绝了，但同意作为朋友相处。

If in the penal farm, you were sure to be criticized.

要是在劳改农场，你等着挨绳子吧！