{"id":3258,"date":"2016-07-23T14:44:15","date_gmt":"2016-07-23T14:44:15","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=3258"},"modified":"2016-07-23T15:08:51","modified_gmt":"2016-07-23T15:08:51","slug":"diagnosticos-se-definen-gracias-a-genomica","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2016\/07\/23\/diagnosticos-se-definen-gracias-a-genomica\/","title":{"rendered":"Diagn\u00f3sticos se definen gracias a gen\u00f3mica"},"content":{"rendered":"<p style=\"text-align: justify\"><a href=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2016\/07\/Dx.jpg\"><img loading=\"lazy\" class=\"alignleft size-full wp-image-3291\" style=\"border-width: 1px;margin: 5px\" src=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2016\/07\/Dx.jpg\" alt=\"Microsoft PowerPoint - Figures 1\" width=\"85\" height=\"67\" \/><\/a>Son varios los diagn\u00f3sticos definidos gracias a las tecnolog\u00edas \u00f3micas. Puede leer algunos ejemplos en:<br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.cmaj.ca\/content\/early\/2016\/05\/30\/cmaj.150823.long\" target=\"_blank\">Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.nature.com\/mp\/journal\/vaop\/ncurrent\/full\/mp2016113a.html\" target=\"_blank\">Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.nature.com\/gim\/journal\/v18\/n7\/full\/gim2015142a.html\" target=\"_blank\">Molecular diagnostic experience of whole-exome sequencing in adult patients<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Son varios los diagn\u00f3sticos definidos gracias a las tecnolog\u00edas \u00f3micas. Puede leer algunos ejemplos en: &#8211; Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit &#8211; Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield &#8211; Molecular diagnostic experience of whole-exome sequencing in adult patients<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[14,15,23,25],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3258"}],"collection":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/users\/125"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/comments?post=3258"}],"version-history":[{"count":3,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3258\/revisions"}],"predecessor-version":[{"id":3293,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3258\/revisions\/3293"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=3258"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=3258"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=3258"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}