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<oembed><version>1.0</version><provider_name>Scule archive</provider_name><provider_url>https://sites.exeter.ac.uk/scule</provider_url><author_name>Dan Lott</author_name><author_url>https://sites.exeter.ac.uk/scule/author/dan-lott/</author_url><title>Recontacting in Mainstreaming Genetics - Scule archive</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="RjJOg4O93F"&gt;&lt;a href="https://sites.exeter.ac.uk/scule/2018/07/05/recontacting-in-mainstreaming-genetics/"&gt;Recontacting in Mainstreaming Genetics&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://sites.exeter.ac.uk/scule/2018/07/05/recontacting-in-mainstreaming-genetics/embed/#?secret=RjJOg4O93F" width="600" height="338" title="&#x201C;Recontacting in Mainstreaming Genetics&#x201D; &#x2014; Scule archive" data-secret="RjJOg4O93F" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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</html><thumbnail_url/><thumbnail_width/><thumbnail_height/><description>Is there a professional duty or responsibility to recontact patients for whom providers hold genetic or genomic information? Do patients and health care providers share responsibility for being aware of new developments relevant to the patient&#x2019;s genome? Do different health care specialties now ordering genetic tests share understandings regarding managing genetic information, which in clinical [&hellip;]</description></oembed>
