{"id":4583,"date":"2020-02-11T04:48:05","date_gmt":"2020-02-11T04:48:05","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=4583"},"modified":"2020-02-15T04:51:18","modified_gmt":"2020-02-15T04:51:18","slug":"nuevas-asociaciones-mutaciones-polimorfismos-insuficiencia-cardiaca-autismo-alcoholismo","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2020\/02\/11\/nuevas-asociaciones-mutaciones-polimorfismos-insuficiencia-cardiaca-autismo-alcoholismo\/","title":{"rendered":"Nuevas asociaciones, mutaciones, polimorfismos: insuficiencia cardiaca, autismo, alcoholismo, &#8230;"},"content":{"rendered":"<p style=\"text-align: justify\">&#8211; G<a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41467-019-13690-5\" target=\"_blank\">enome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41467-019-13690-5\" target=\"_blank\">The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/jamanetwork.com\/journals\/jamanetworkopen\/fullarticle\/2760446\" target=\"_blank\">Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability<\/a><br \/>\n&#8211; <a href=\"https:\/\/jamanetwork.com\/journals\/jamanetworkopen\/fullarticle\/2759847\" target=\"_blank\">Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations<\/a><br \/>\n&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/advances.sciencemag.org\/content\/6\/3\/eaay5034\" target=\"_blank\">Functional validity, role, and implications of heavy alcohol consumption genetic loci<\/a><\/p>\n<p style=\"text-align: justify\">&#8211; <a title=\"Texto completo en ingl\u00e9s\" href=\"https:\/\/www.nature.com\/articles\/s41467-020-14625-1\" target=\"_blank\">Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>&#8211; Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure &#8211; The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderly &#8211; Association of Genetic Risks With Autism Spectrum Disorder and Early Neurodevelopmental Delays Among Children Without Intellectual Disability &#8211; Copy Number Variation and Clinical [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[13,15,21,23,25,26,29],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4583"}],"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=4583"}],"version-history":[{"count":4,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4583\/revisions"}],"predecessor-version":[{"id":4618,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4583\/revisions\/4618"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=4583"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=4583"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=4583"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}