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*** Genetics 4 Medics featured in The Lancet (Sep, 2011)

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*** Compiled by doctors from Clinical Genetics, Pediatrics & Cardiology backgrounds

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*** NEW*** Version 3.0

1. Conditions section completely revised and updated as of January 2014.

2. Diagrams added.

3. Links to PubMed review articles.

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Genetics 4 Medics application is intended to facilitate the learning process as well as to refresh the knowledge which has already been acquired. We hope this will be useful to students and practicing clinicians alike. 

*** NOTE: In the free version, the user will have access to 50 Genetic conditions, 50 Clues, 3 Chromosomes in the mapping section and the questions in the Gene Teaser section. To unlock all features, please upgrade to the full version by an in-app purchase. 

*** The free version is ad supported

We have designed this app to be used as a mini eBook with five sections.

1. Genetic Conditions

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In this section, we have described more than 200 genetic conditions.  The objective was to help find information on conditions which are not so uncommon.  

Each condition has the following headings:

• Background & Genetics: This includes a brief description of the genetic cause (gene mutation, chromosomal location etc) and inheritance pattern of the condition.

• Salient Features:  This describes the salient clinical features of a condition. We have included only the clinical features commonly associated with the condition. We have NOT included rare associations. 

• Links to external online resources: We have provided links to Wikipedia, Google Images and YouTube for majority of conditions. NOTE: The material in these external websites are not under our control, and we are not responsible its content. Access to these websites will need an active internet connection either via WiFi or internet data plan. 

Condition Mapping

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In this section, we have mapped a condition to its chromosomal locus. We have mainly included conditions caused by single gene defect. Clicking on the titles will open up the description page.

Note: The chromosome diagrams are only pictorial representations to facilitate visual learning and memory. They do not represent exact G banding pattern and are not drawn to scale. 

3. Clues

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We have included about 150 clinical features which are clues to some of the conditions described in this application. Some clinical features may be shared by different conditions.   Clicking on a feature provides links to these conditions. However, as we have only used data from the ‘Salient features’ section, this is not an exhaustive list. Please refer to standard genetic textbooks for a complete list of conditions associated with a particular clinical symptom or sign.

4. Gene Teasers

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Food for your genes! Try out these questions in your spare time. We plan to update this section regularly with a new question. A notification will be sent whenever this section is updated with a new question. The title of the case scenario will automatically be updated in this section. The user will be able to download the case by selecting the download icon next to the title. NOTE: An active internet connection will be needed for the regular updates as well as to download the cases.   

5. Basics

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In this section, we have described some basic genetic concepts and genetic investigations using simple terminology. 

Genetics 4 Medics application should only be used for educational purposes and NOT as a diagnostic tool. For help with diagnosing a genetic condition, please take advice from an experienced Clinical Geneticist. 

Full Terms & Conditions available on downloading the app. Users must agree to these Terms & Conditions prior to use.

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Please contact us for support or feedback - <a href="mailto:contact@apps4medics.com">contact@apps4medics.com</a>

</div> <div jsname="WJz9Hc" style="display:none">***遗传学4医务人员精选于柳叶刀（九月，2011）

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***编译通过临床遗传学，儿科和心内科的医生背景

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*** ***新的3.0版本

1.条件部分完全修订和更新2014年一月。

2.添加图表。

3.链接到考研复习的文章。

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遗传学4医务人员申请旨在促进学习过程以及刷新已经被获得的知识。我们希望这将是有用的学生和临床医生的一致好评。

***注：在自由版本，用户将有机会获得50遗传条件，50线索，3染色体在映射部和在基因预告节中的问题。要解锁所有功能，请通过应用程序内购买升级到完整版本。

***免费版的广告支持

我们设计这个程序被用来作为一个小型的电子书具有五段。

1.遗传疾病

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在本节中，我们描述了200多个基因的条件。我们的目标是帮助找到它不那么罕见情况的信息。

每个条件具有以下标题：

•背景和遗传学：这包括遗传原因的简要说明（基因突变，染色体定位等）和遗传模式的条件。

•显着特点：它描述的条件显着的临床特征。这里只包含通常与条件相关的临床特征。我们还没有包括罕见的关联。

•链接到外部的在线资源：我们提供的链接维基百科，谷歌图片和YouTube的大部分条件。注意：在这些外部网站的材料不在我们的控制之下，我们不负责其内容。访问这些网站都需要通过WiFi或互联网数据计划激活的Internet连接无论是。

条件映射

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在本节中，我们已经映射了一个条件，它的染色体基因。我们主要造成包括单基因缺陷的条件。点击标题就会打开描述页面。

注意：染色体图表仅仅图形表示，以方便视觉学习和记忆。它们不代表确切G显带模式，并且不按比例绘制。

3.线索

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我们已经包括大约150临床特征它们是线索的一些在本申请中所述的条件。一些临床特征可以通过不同的条件共享。点击一个功能提供链接，这些条件。然而，正如我们只能从“突出特点”部分使用的数据，这不是一个详尽的清单。请参考标准遗传教科书与特定临床症状或迹象相关的病症的完整列表。

4.基因玩笑

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食物你的基因！请试着在你的业余时间这些问题。我们计划定期与一个新的问题更新此节。每当这个部分是一个新的问题，更新的通知将被发送。的情况下的标题将自动在本节进行更新。用户将能够通过选择标题旁下载图标下载的情况。注：可用的Internet连接将需要定期更新，以及下载的情况。

5.基础知识

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在本节中，我们已经介绍了使用简单的术语的一些基本概念，基因和遗传的调查。

遗传学4医务人员的应用程序应该只用于教育目的，不作为诊断工具。为了帮助诊断遗传性疾病，请有经验的临床遗传学家纳谏。

全部条款和条件可下载的应用程序。用户必须同意这些条款和条件后才能使用。

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