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   <channel>
      <title>Genetics Home Reference</title>
      <link>http://www.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, 17 Jun 2013 00:00:00 Z</lastBuildDate>
      <dc:publisher>US National Library of Medicine</dc:publisher>
      <dc:rights>Subject to "Terms of Use" at http://www.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://www.ghr.nlm.nih.gov/html/images/genetics_home_reference_rss.gif</url>
         <title>Genetics Home Reference</title>
         <link>http://www.ghr.nlm.nih.gov/?wf=1</link>
         <width>88</width>
         <height>31</height>
      </image>
      <ttl>1440</ttl>
      <item>
         <title>Pol III-related leukodystrophy</title>
         <link>http://www.ghr.nlm.nih.gov/condition/pol-iii-related-leukodystrophy?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/pol-iii-related-leukodystrophy</guid>
         <description>Pol III-related leukodystrophy and its relationship with genes POLR3A and POLR3B have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, Gene Reviews, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 17 Jun 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>medullary cystic kidney disease type 1</title>
         <link>http://www.ghr.nlm.nih.gov/condition/medullary-cystic-kidney-disease-type-1?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/medullary-cystic-kidney-disease-type-1</guid>
         <description>Medullary cystic kidney disease type 1 and its relationship with gene MUC1 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 17 Jun 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>antiphospholipid syndrome</title>
         <link>http://www.ghr.nlm.nih.gov/condition/antiphospholipid-syndrome?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/antiphospholipid-syndrome</guid>
         <description>Antiphospholipid syndrome has been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 10 Jun 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>What does it mean to have a genetic predisposition to a disease?</title>
         <link>http://www.ghr.nlm.nih.gov/handbook/mutationsanddisorders/predisposition?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/handbook/mutationsanddisorders/predisposition</guid>
         <description>A new section has been added to the Handbook.  The Handbook presents basic information about genetics in clear language and provides links to other online resources.</description>
         <pubDate>Mon, 03 Jun 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>Weaver syndrome</title>
         <link>http://www.ghr.nlm.nih.gov/condition/weaver-syndrome?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/weaver-syndrome</guid>
         <description>Weaver syndrome and its relationship with genes EZH2 and NSD1 have been added to Genetics Home Reference.  Web links to MedlinePlus, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Wed, 29 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>critical congenital heart disease</title>
         <link>http://www.ghr.nlm.nih.gov/condition/critical-congenital-heart-disease?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/critical-congenital-heart-disease</guid>
         <description>Critical congenital heart disease and its relationship with gene GJA1 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Wed, 29 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis</title>
         <link>http://www.ghr.nlm.nih.gov/condition/naegeli-franceschetti-jadassohn-syndrome-dermatopathia-pigmentosa-reticularis?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/naegeli-franceschetti-jadassohn-syndrome-dermatopathia-pigmentosa-reticularis</guid>
         <description>Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis and its relationship with gene KRT14 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Wed, 29 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>benign chronic pemphigus</title>
         <link>http://www.ghr.nlm.nih.gov/condition/benign-chronic-pemphigus?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/benign-chronic-pemphigus</guid>
         <description>Benign chronic pemphigus and its relationship with gene ATP2C1 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, NIH publications, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Wed, 29 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>Partington syndrome</title>
         <link>http://www.ghr.nlm.nih.gov/condition/partington-syndrome?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/partington-syndrome</guid>
         <description>Partington syndrome and its relationship with gene ARX have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Wed, 29 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>renal tubular dysgenesis</title>
         <link>http://www.ghr.nlm.nih.gov/condition/renal-tubular-dysgenesis?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/renal-tubular-dysgenesis</guid>
         <description>Renal tubular dysgenesis and its relationship with genes ACE, AGT, AGTR1, and REN have been added to Genetics Home Reference.  Web links to MedlinePlus, NIH publications, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Wed, 29 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>Coffin-Siris syndrome</title>
         <link>http://www.ghr.nlm.nih.gov/condition/coffin-siris-syndrome?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/coffin-siris-syndrome</guid>
         <description>Coffin-Siris syndrome and its relationship with genes ARID1A, ARID1B, SMARCA4, SMARCB1, and SMARCE1 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, patient support web sites, Gene Reviews, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 20 May 2013 00:00:00 Z</pubDate>
      </item>
      <item>
         <title>factor V deficiency</title>
         <link>http://www.ghr.nlm.nih.gov/condition/factor-v-deficiency?wf=1</link>
         <guid>http://www.ghr.nlm.nih.gov/condition/factor-v-deficiency</guid>
         <description>Factor V deficiency and its relationship with gene F5 have been added to Genetics Home Reference.  Web links to MedlinePlus, Genetic and Rare Diseases Information Center, patient support web sites, Genetic Testing Registry, ClinicalTrials.gov, PubMed, and OMIM are included.</description>
         <pubDate>Mon, 20 May 2013 00:00:00 Z</pubDate>
      </item>
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