The incidence of VWS is 1-3/ 30000, penetrance is 80-94%.

Analysis results show that VWS technology can be well done Web page segmentation, solve the problem of web pages displayed in the phone rightly and has a better user experience.

分析结果表明，VWS技术可出色地完成Web网页分割，实现针对PC端设计的网页在手机中的正常显示，并且具有较好的用户体验。

The complaint alleges the group fitted nearly 600000 VWs, Audis and Porsches with diesel engines that contained illegal "defeat devices" and caused emissions to exceed EPA standards.

诉状声称，大众为近60万辆大众、奥迪（Audi）和保时捷（Porsche）车辆安装了包含非法“减效装置”的柴油发动机，使这些车辆的排放超出美国国家环保局的标准。

Many of the technologies, such as the liberal use of carbon fiber, might make be used for other VWS, helping to make them lighter and more efficient.

这辆车采用的很多技术，比如大量碳纤维材料，可能会用到大众旗下的其他车型上，让它们变得更轻、更高效。

To simplify the FMS controller design, a concept of virtual workstation ( VWS) is introduced. Applying VWS, part of control functions of FMS controller can be transferred to the lower workstation level.

为简化FMS控制系统的设计，提出了虚拟工作站的概念与方法，将FMS控制器的部分控制功能下放到低层的工作站控制层。

And someone had been apprehended cutting down trees, a row of elms broken-backed among the VWs and Valiants.

有人因砍树被捕，一排被腰斩的榆树倒在大众和威廉中间。

In a letter circulating online, an association representing dealers that sell imported VWs have complained of persistently high sales targets, despite slowing economic growth and intense competition.

在网上流传的一份信件中，代表大众进口车经销商的一个协会抱怨称，尽管经济增长放缓和竞争激烈，但大众仍坚持过高的销售目标。

How to find information about human genes and hereditary disorders with OMIM

如何利用OMIM获取人类基因与遗传失调信息

Van der Woude syndrome ( VWS, OMIM 119300) is an autosomal dominant craniofacial disorder characterized by pits of the lower lip, hypodontia and cleft lip and/ or cleft palate.

范德伍兹综合征（Van der Woude syndrome，VWS，OMIM119300）是一种常染色体显性遗传病。其特征是家族性下唇瘘复合唇裂或腭裂，1／4的患者伴有缺牙（Hypodontia）。

Background Familial benign chronic pemphigus or Hailey-Hailey disease ( HHD; OMIM 169600) is a rare autosomal dominant cutaneous disorder characterized by recurrent vesicles and erosions mainly in intertriginous areas.

研究背景：家族性慢性良性天疱疮，又称Hailey-Hailey病（HHD，OMIM169600）是一种罕见的常染色体显性遗传性皮肤病。

Create a web-enabled script that given a locus link ID returns all the gene polymorphisms, OMIM citations associated with that gene.

建立一个web上使用的、一个地点链接的ID的脚本，可得到所有的基因多态、和那些基因相关的OMIM引文。

Reorganizing Analysis of Genetic Research Materials Related to Tongue Diagnosis in OMIM

OMIM中与舌诊相关的基因研究资料的整理分析

Osteogenesis imperfecta ( OMIM 166200) is an autosomal dominant disorder characterized by bone fragility and abnormalities of connective tissue.

成骨不全病（OMIM166200）是一种常染色体显性遗传病，其临床表现以骨折及结缔组织异常为特征。

There are two methods for the disease phenotype similarity in this article. They are separately based on the vector space and based on the scene pattern. By the two methods we can obtain the similarity of disease phenotype in OMIM text.

分别利用基于向量空间的疾病表型相似度挖掘方法、基于情景模式的疾病表型相似度挖掘方法，通过这两种方法得到OMIM文本中疾病表型的相似度。

Sequence homology analysis of 12 specific fragments was done through BLAST at the NCBI web.

对12个差异片段进行核苷酸序列相似性比对和功能分析。

Sequence and intron analysis were based on NCBI database and EMBL database resource.

通过NCBI数据库资源对醛缩酶内含子的分布及大小进行比较分析。

After the Sequencing Blast in the NCBI database, 141 effective results had been showed.

测序结果在NCBI数据库中经Blast比对共得到141个有效比对结果。

The other two were new expressed segments, so highly homologous sequences were not found in NCBI.

其余两条为新发现的表达片段，在NCBI中未发现高度同源序列。

After NCBI blast, no homologous protein was found.

在NCBI中比对没有发现符合条件的胞外蛋白。

The team compared these with the US National Center for Biotechnology Information ( NCBI) reference human genome.

他们把这些数据和美国国家生物技术信息中心（NCBI）的参考人类基因组进行了比较。

Making Use of My NCBI and RSS to Provide Information Service for Sci-tec Researchers by Libraries

图书馆利用My NCBI和RSS为科研人员提供信息服务