http://www.ghr.nlm.nih.gov/?wf=1 The US National Library of Medicine's web site for consumer information about genetic conditions and the genes or chromosomes responsible for those conditions. http://blogs.law.harvard.edu/tech/rss en-US Fri, 20 Nov 2009 00:00:00 Z US National Library of Medicine Subject to "Terms of Use" at http://www.ghr.nlm.nih.gov/TermsAndConditions?wf=1 Health/Conditions_and_Diseases/Genetic_Disorders Health/Resources/Consumer_Information Health/Education/Patient_Education http://www.ghr.nlm.nih.gov/html/images/genetics_home_reference_rss.gif http://www.ghr.nlm.nih.gov/?wf=1 88 31 1440 http://www.ghr.nlm.nih.gov/condition=22q112duplication?wf=1 http://www.ghr.nlm.nih.gov/condition=22q112duplication 22q11.2 duplication and its relationship with chromosome 22 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. Fri, 20 Nov 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=zap70relatedseverecombinedimmunodeficiency?wf=1 http://www.ghr.nlm.nih.gov/condition=zap70relatedseverecombinedimmunodeficiency ZAP70-related severe combined immunodeficiency and its relationship with gene ZAP70 have been added to Genetics Home Reference. Web links to MedlinePlus, NIH publications, Genes and Disease, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included. Fri, 20 Nov 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=millerdiekersyndrome?wf=1 http://www.ghr.nlm.nih.gov/condition=millerdiekersyndrome Miller-Dieker syndrome and its relationship with chromosome 17 and genes PAFAH1B1 and YWHAE 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. Mon, 16 Nov 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=16p112deletionsyndrome?wf=1 http://www.ghr.nlm.nih.gov/condition=16p112deletionsyndrome 16p11.2 deletion syndrome and its relationship with chromosome 16 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. Fri, 06 Nov 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=jacobsensyndrome?wf=1 http://www.ghr.nlm.nih.gov/condition=jacobsensyndrome Jacobsen syndrome and its relationship with chromosome 11 have been added to Genetics Home Reference. Web links to MedlinePlus, patient support web sites, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included. Fri, 30 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=proteincdeficiency?wf=1 http://www.ghr.nlm.nih.gov/condition=proteincdeficiency Protein C deficiency and its relationship with gene PROC 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. Fri, 30 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=proteinsdeficiency?wf=1 http://www.ghr.nlm.nih.gov/condition=proteinsdeficiency Protein S deficiency and its relationship with gene PROS1 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. Fri, 30 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=microphthalmiawithlinearskindefectssyndrome?wf=1 http://www.ghr.nlm.nih.gov/condition=microphthalmiawithlinearskindefectssyndrome Microphthalmia with linear skin defects syndrome and its relationship with chromosome X and gene HCCS 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. Fri, 23 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=diamondblackfananemia?wf=1 http://www.ghr.nlm.nih.gov/condition=diamondblackfananemia Diamond-Blackfan anemia and its relationship with genes RPL5, RPL11, RPL35A, RPS7, RPS17, RPS19, and RPS24 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. Fri, 09 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=vldlrassociatedcerebellarhypoplasia?wf=1 http://www.ghr.nlm.nih.gov/condition=vldlrassociatedcerebellarhypoplasia VLDLR-associated cerebellar hypoplasia and its relationship with gene VLDLR 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. Fri, 09 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=22q133deletionsyndrome?wf=1 http://www.ghr.nlm.nih.gov/condition=22q133deletionsyndrome 22q13.3 deletion syndrome and its relationship with chromosome 22 and gene SHANK3 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. Fri, 02 Oct 2009 00:00:00 Z http://www.ghr.nlm.nih.gov/condition=feingoldsyndrome?wf=1 http://www.ghr.nlm.nih.gov/condition=feingoldsyndrome Feingold syndrome and its relationship with gene MYCN have been added to Genetics Home Reference. Web links to MedlinePlus, patient support web sites, Gene Reviews, Gene Tests, ClinicalTrials.gov, PubMed, and OMIM are included. Fri, 02 Oct 2009 00:00:00 Z