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      <title>Genomics Case 2 Question 2D by </title>
      <link>https://padlet.com/haspelr/uvdx5g71p9j516fq</link>
      <description>You receive the molecular testing report at http://bit.ly/moleculartestingreport and note an STK11 Q170* variant ((STK11):c.508C&gt;T (p.Gln170Ter)). Using ClinGen (https://www.clinicalgenome.org/).</description>
      <language>en-us</language>
      <pubDate>2021-09-16 15:08:02 UTC</pubDate>
      <lastBuildDate>2021-10-28 12:31:12 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>Differential Diagnosis</title>
         <author>haspelr</author>
         <link>https://padlet.com/haspelr/uvdx5g71p9j516fq/wish/1746272647</link>
         <description><![CDATA[<div><strong>What are other diseases in the differential diagnosis of Peutz-Jeghers Syndrome? </strong><em>(Hint: Through the STK11 ClinGen entry, use GeneReviews and look at table 3 in the article)</em></div><div>_______________________________________<br>To create a new post, double-click on a blank space or click the plus sign in the lower right-hand corner. You can ignore the&nbsp; Subject line if you prefer. In the body (under the icons), type your response.&nbsp; Click "Publish" when you are finished. You can resize your posts by dragging on the edges.<strong><br><br></strong><a href="https://devryuniversity.padlet.org/eanderson90/genomics21"><strong>RETURN to Main Padlet here</strong></a><strong>.</strong></div>]]></description>
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         <pubDate>2021-09-16 15:08:02 UTC</pubDate>
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