<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[RSS Feed]]></title><description><![CDATA[RSS Feed]]></description><link>http://direct.ecency.com</link><image><url>http://direct.ecency.com/logo512.png</url><title>RSS Feed</title><link>http://direct.ecency.com</link></image><generator>RSS for Node</generator><lastBuildDate>Fri, 24 Apr 2026 11:28:15 GMT</lastBuildDate><atom:link href="http://direct.ecency.com/created/22q112/rss.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[22q11.2 duplication syndrome]]></title><description><![CDATA[The most frequent reported symptoms in patients with duplication of 22q11.2 duplication syndrome are mental retardation/learning disabilility (97% of patients), delayed psychomotor development (67% of]]></description><link>http://direct.ecency.com/22q112/@karthikmbbs2/22q11-2-duplication-syndrome-4ddf1d0239ddf</link><guid isPermaLink="true">http://direct.ecency.com/22q112/@karthikmbbs2/22q11-2-duplication-syndrome-4ddf1d0239ddf</guid><category><![CDATA[22q112]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Tue, 08 May 2018 16:41:24 GMT</pubDate></item><item><title><![CDATA[22q11.2 distal deletion syndrome]]></title><description><![CDATA[22q11.2 distal deletion syndrome is a rare genetic condition caused by a tiny missing part of one of the body’s 46 chromosomes – chromosome 22. 22q11.2 distal deletion syndrome appears to be a recurrent]]></description><link>http://direct.ecency.com/22q112/@karthikmbbs/22q11-2-distal-deletion-syndrome-80d4708e67694</link><guid isPermaLink="true">http://direct.ecency.com/22q112/@karthikmbbs/22q11-2-distal-deletion-syndrome-80d4708e67694</guid><category><![CDATA[22q112]]></category><dc:creator><![CDATA[karthikmbbs]]></dc:creator><pubDate>Tue, 08 May 2018 16:40:30 GMT</pubDate></item></channel></rss>