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<title>Medical Xpress: PHYSorg news tagged with: genetic mapping</title>
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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>A GPS in your DNA: Research says genetics can reveal your geographic ancestral origin</title>
   	 <description>While your DNA is unique, it also tells the tale of your family line. It carries the genetic history of your ancestors down through the generations. Now, says a Tel Aviv University researcher, it's also possible to use it as a map to your family's past.</description>
	  <link>http://medicalxpress.com/news/2012-08-gps-dna-genetics-reveal-geographic.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 16 Aug 2012 10:10:01 EST</pubDate>
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     <title>Stanford researcher to expand DNA database by adding Latin Americans</title>
   	 <description>(Medical Xpress) -- Genetic mapping has led scientists to a better understanding of human disease and how to fight ailments like diabetes, mental illness and cancer.</description>
	  <link>http://medicalxpress.com/news/2012-07-stanford-dna-database-adding-latin.html</link>
	 <category>Genetics</category>
	 <pubDate>Fri, 20 Jul 2012 10:15:06 EST</pubDate>
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     <title>Rare muscular dystrophy gene mutations discovered</title>
   	 <description>(Medical Xpress) -- Research co-led by Radboud University Nijmegen Medical Centre and the Wellcome Trust Sanger Institute has revealed gene mutations that account for 15 per cent of all babies born with Walker-Warburg syndrome, a rare congenital muscular dystrophy. The syndrome, which is associated with muscle wasting, brain and eye abnormalities, is fatal and most babies do not live beyond two years. A key symptom is hydrocephalus - having an enlarged brain filled with excess fluid.</description>
	  <link>http://medicalxpress.com/news/2012-04-rare-muscular-dystrophy-gene-mutations.html</link>
	 <category>Genetics</category>
	 <pubDate>Tue, 24 Apr 2012 09:20:01 EST</pubDate>
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     <title>New lab mice cut search for genetic links to disease by more than a decade</title>
   	 <description>With a 95 percent genomic similarity to humans, mice have long been used to learn about the genetic causes of human disease. Once researchers can shine a light on the genetic factors that cause disease in mice, they can start to develop prevention and treatment options to protect the human population.</description>
	  <link>http://medicalxpress.com/news/2012-04-lab-mice-genetic-links-disease.html</link>
	 <category>Genetics</category>
	 <pubDate>Thu, 05 Apr 2012 11:25:38 EST</pubDate>
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