{"id":2323,"date":"2017-09-17T20:36:27","date_gmt":"2017-09-17T20:36:27","guid":{"rendered":"https:\/\/www.primarycaregenetics.org\/?page_id=2323"},"modified":"2017-09-17T20:48:57","modified_gmt":"2017-09-17T20:48:57","slug":"hjartasjukdomar-i-grunnthjonustu","status":"publish","type":"page","link":"https:\/\/www.primarycaregenetics.org\/?page_id=2323&lang=is","title":{"rendered":"Nokkur gagnleg d\u00e6mi"},"content":{"rendered":"<p>H\u00e9r er hlekkur \u00ed uppl\u00fdsingar sem \u00e6tla\u00f0ar eru heimilisl\u00e6knum og lj\u00f3sm\u00e6\u00f0rum. \u00deessar uppl\u00fdsingar byggja \u00e1 fimm mismunandi tilfellum og eru \u00e1 ensku: (cystic fibrosis, Down syndrome, the child with an learning disability, consanguinity and an X-linked disorder).<\/p>\n<p><a href=\"http:\/\/www.ucd.ie\/medicine\/rarediseases\/informationforgps\">http:\/\/www.ucd.ie\/medicine\/rarediseases\/informationforgps<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>H\u00e9r er hlekkur \u00ed uppl\u00fdsingar sem \u00e6tla\u00f0ar eru heimilisl\u00e6knum og lj\u00f3sm\u00e6\u00f0rum. \u00deessar uppl\u00fdsingar byggja \u00e1 fimm mismunandi tilfellum og eru \u00e1 ensku: (cystic fibrosis, Down syndrome, the child with an learning disability, consanguinity and an X-linked disorder). http:\/\/www.ucd.ie\/medicine\/rarediseases\/informationforgps<\/p>\n","protected":false},"author":3,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"ngg_post_thumbnail":0},"_links":{"self":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/2323"}],"collection":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=2323"}],"version-history":[{"count":2,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/2323\/revisions"}],"predecessor-version":[{"id":2342,"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=\/wp\/v2\/pages\/2323\/revisions\/2342"}],"wp:attachment":[{"href":"https:\/\/www.primarycaregenetics.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=2323"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}