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<title>Medical Xpress: PHYSorg news tagged with: genetic syndromes</title>
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     <title>Researchers identify mutation that causes short-sightedness and hearing loss</title>
   	 <description>(Medical Xpress)—Researchers have identified a new disorder caused by a genetic mutation that leads to short sightedness and deafness. They say the new link between the two sensory problems could lead to better understanding of the disease mechanism of each.</description>
     <link>http://medicalxpress.com/news/2013-04-mutation-short-sightedness-loss.html</link>
	 <category>Genetics</category>
	 <pubDate>Mon, 08 Apr 2013 08:31:11 EST</pubDate>
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     <title>Whole-exome sequencing identifies inherited mutations in autism</title>
   	 <description>While autism clearly runs in some families, few inherited genetic causes have been found. A major reason is that these causes are so varied that it's hard to find enough people with a given mutation to establish a clear pattern. Researchers at Boston Children's Hospital have pinpointed several inherited mutations—among the first to be identified—through an unusual approach: using whole-exome sequencing to study large Middle Eastern families with autism.</description>
     <link>http://medicalxpress.com/news/2013-01-whole-exome-sequencing-inherited-mutations-autism.html</link>
	 <category>Autism spectrum disorders</category>
	 <pubDate>Wed, 23 Jan 2013 12:00:01 EST</pubDate>
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     <title>Research discovers likely basis of birth defect causing premature skull closure in infants</title>
   	 <description>An international team of geneticists, pediatricians, surgeons and epidemiologists from 23 institutions across three continents has identified two areas of the human genome associated with the most common form of non-syndromic craniosynostosis ― premature closure of the bony plates of the skull.</description>
     <link>http://medicalxpress.com/news/2012-11-basis-birth-defect-premature-skull.html</link>
	 <category>Genetics</category>
	 <pubDate>Sun, 18 Nov 2012 13:00:09 EST</pubDate>
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