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      <title>Genetics Home Reference</title>
      <link>http://ghr.nlm.nih.gov/?wf=1</link>
      <description>The US National Library of Medicine's web site for consumer information about genetic conditions and the genes or chromosomes responsible for those conditions.</description>
      <docs>http://blogs.law.harvard.edu/tech/rss</docs>
      <language>en-US</language>
      <lastBuildDate>Mon, 14 May 2012 00:00:00 Z</lastBuildDate>
      <dc:publisher>US National Library of Medicine</dc:publisher>
      <dc:rights>Subject to "Terms of Use" at http://ghr.nlm.nih.gov/TermsAndConditions?wf=1</dc:rights>
      <category domain="http://dmoz.org">Health/Conditions_and_Diseases/Genetic_Disorders</category>
      <category domain="http://dmoz.org">Health/Resources/Consumer_Information</category>
      <category domain="http://dmoz.org">Health/Education/Patient_Education</category>
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         <url>http://ghr.nlm.nih.gov/html/images/genetics_home_reference_rss.gif</url>
         <title>Genetics Home Reference</title>
         <link>http://ghr.nlm.nih.gov/?wf=1</link>
         <width>88</width>
         <height>31</height>
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      <ttl>1440</ttl>
      <item>
         <title>familial acute myeloid leukemia with mutated CEBPA</title>
         <link>http://ghr.nlm.nih.gov/condition/familial-acute-myeloid-leukemia-with-mutated-cebpa?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/familial-acute-myeloid-leukemia-with-mutated-cebpa</guid>
         <description>Familial acute myeloid leukemia with mutated CEBPA and its relationship with gene CEBPA have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 14 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>dopa-responsive dystonia</title>
         <link>http://ghr.nlm.nih.gov/condition/dopa-responsive-dystonia?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/dopa-responsive-dystonia</guid>
         <description>Dopa-responsive dystonia and its relationship with genes GCH1, SPR, and TH have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 14 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>supravalvular aortic stenosis</title>
         <link>http://ghr.nlm.nih.gov/condition/supravalvular-aortic-stenosis?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/supravalvular-aortic-stenosis</guid>
         <description>Supravalvular aortic stenosis and its relationship with gene ELN have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 07 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>lattice corneal dystrophy type II</title>
         <link>http://ghr.nlm.nih.gov/condition/lattice-corneal-dystrophy-type-ii?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/lattice-corneal-dystrophy-type-ii</guid>
         <description>Lattice corneal dystrophy type II and its relationship with gene GSN have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 07 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>hereditary cerebral amyloid angiopathy</title>
         <link>http://ghr.nlm.nih.gov/condition/hereditary-cerebral-amyloid-angiopathy?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/hereditary-cerebral-amyloid-angiopathy</guid>
         <description>Hereditary cerebral amyloid angiopathy and its relationship with genes APP, CST3, and ITM2B have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 07 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>lattice corneal dystrophy type I</title>
         <link>http://ghr.nlm.nih.gov/condition/lattice-corneal-dystrophy-type-i?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/lattice-corneal-dystrophy-type-i</guid>
         <description>Lattice corneal dystrophy type I and its relationship with gene TGFBI have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 07 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>tarsal-carpal coalition syndrome</title>
         <link>http://ghr.nlm.nih.gov/condition/tarsal-carpal-coalition-syndrome?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/tarsal-carpal-coalition-syndrome</guid>
         <description>Tarsal-carpal coalition syndrome and its relationship with gene NOG have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 07 May 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>metatropic dysplasia</title>
         <link>http://ghr.nlm.nih.gov/condition/metatropic-dysplasia?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/metatropic-dysplasia</guid>
         <description>Metatropic dysplasia and its relationship with gene TRPV4 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 30 Apr 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>purine nucleoside phosphorylase deficiency</title>
         <link>http://ghr.nlm.nih.gov/condition/purine-nucleoside-phosphorylase-deficiency?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/purine-nucleoside-phosphorylase-deficiency</guid>
         <description>Purine nucleoside phosphorylase deficiency and its relationship with gene PNP have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, Genes and Disease, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 30 Apr 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>intranuclear rod myopathy</title>
         <link>http://ghr.nlm.nih.gov/condition/intranuclear-rod-myopathy?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/intranuclear-rod-myopathy</guid>
         <description>Intranuclear rod myopathy and its relationship with gene ACTA1 have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 30 Apr 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>actin-accumulation myopathy</title>
         <link>http://ghr.nlm.nih.gov/condition/actin-accumulation-myopathy?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/actin-accumulation-myopathy</guid>
         <description>Actin-accumulation myopathy and its relationship with gene ACTA1 have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 30 Apr 2012 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>cap myopathy</title>
         <link>http://ghr.nlm.nih.gov/condition/cap-myopathy?wf=1</link>
         <guid>http://ghr.nlm.nih.gov/condition/cap-myopathy</guid>
         <description>Cap myopathy and its relationship with genes ACTA1, TPM2, and TPM3 have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 30 Apr 2012 00:00:00 Z</pubDate>
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