遗传学

The human Y chromosome is paternally inherited in a haplotype model.

人类Y染色体为正常男性特有、其大部分非重组区呈父系单倍型遗传等特点，使得Y染色体特异的多态性遗传标记成为人类学、群体遗传学及法。。。

The human Y chromosome is paternally inherited in a haplotype model. This feature make the Y-specific polymorphic markers are very useful in different fields of science, including genealogy, population genetics and forensic science.

人类Y染色体为正常男性特有、其大部分非重组区呈父系单倍型遗传等特点，使得Y染色体特异的多态性遗传标记成为人类学、群体遗传学及法医学等领域中非常有用的工具。

Continue a sharpening therefore , only with the immunology , biochemistry , genetics , microanatomy , pathology, and discipline connection and combined efforts, make use of advanced technology other, especially molecular biology technology, ability accelerates development of Medical Microbiology , is that the pathogene soon, controlling and wiping out healthy various endangering human being makes contribution.

因此，只有继续加强与免疫学，生物化学，遗传学，组织学，病理学，和其他学科的联系和协作，利用先进的技术，特别是分子生物学技术，才能加快医学微生物学的发展，为早日控制和消灭危害人类健康的各种病原体作出贡献。

Huntington's disease known as inherited chronic chorea is an autosomal dominant disorder. After collection of a large HD pedigree from HuBei, the molecular diagnosis of the patients, the pre-symptomatic diagnosis of the persons on risk and the genetic analysis of this pedigree are performed so that the pathogene of this family can be confirmed.

目的：采集湖北省宜昌市秭归县一大Huntington舞蹈病家系，对患者进行基因诊断，对有发病可能性的成员进行预测，同时对该家系进行遗传学分析，验证该家系是否符合Huntington舞蹈病的病因。

Sarah Pavan want to go through the Wednesday routine of scurrying from her genetics class just to make it for the last few minutes of Nebraska's passing .

是否莎拉帕凡想要去的，通过周三的例行们从她的遗传学阶层只是使它为最后几分钟内布拉斯加州s通过。

Does Sarah Pavan want to go through the Wednesday routine of scurrying from her genetics class just to make it for the last few minutes of Nebraska s passing .

是否莎拉帕凡想要去的，通过周三的例行们从她的遗传学阶层只是使它为最后几分钟内布拉斯加州s通过。

The PCC technique would be useful and powerful tools in mosquito cytogenetic study.

PCC技术可成为实用有效的蚊细胞遗传学研究技术。

Some questions about introduction, improvement and utilization for green pod edible pea were also discussed.

最后，从遗传学、生态学和社会学的角度就食荚青豌的引种、改良和利用研究过程中有关问题进行了讨论。

In this study, we recruited a complex NSHI pedigree from Jiangsu province of China.

在本研究中，收集了江苏省一个复杂的非综合征性耳聋家系，并对其进行了分子遗传学研究。

Methods We studied nine children from six families who had neonatal onset of sterile multifocal osteomyelitis, periostitis, and pustulosis.

所有的儿童都有IL1RN基因的遗传学突变，IL1RN基因编码的蛋白质为白细胞介素1受体拮抗剂(IL-1Ra)。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。