{"id":1158,"date":"2013-07-21T23:34:28","date_gmt":"2013-07-22T03:34:28","guid":{"rendered":"http:\/\/blogviejo.sld.cu\/oserranob\/?p=1158"},"modified":"2013-07-21T23:34:28","modified_gmt":"2013-07-22T03:34:28","slug":"genomica-y-bioinformatica-en-diagnostico-del-autismo","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2013\/07\/21\/genomica-y-bioinformatica-en-diagnostico-del-autismo\/","title":{"rendered":"Gen\u00f3mica y bioinform\u00e1tica en diagn\u00f3stico del autismo"},"content":{"rendered":"<p><a href=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2013\/07\/ASD.jpg\"><img loading=\"lazy\" class=\"alignleft size-full wp-image-1219\" style=\"border: 1px solid black;margin: 5px\" src=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2013\/07\/ASD.jpg\" alt=\"\" width=\"105\" height=\"97\" srcset=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2013\/07\/ASD.jpg 485w, https:\/\/blogs.sld.cu\/oserranob\/files\/2013\/07\/ASD-300x277.jpg 300w\" sizes=\"(max-width: 105px) 100vw, 105px\" \/><\/a>La secuenciaci\u00f3n del genoma completo en 32 familias con <a title=\"Informaci\u00f3n sobre la enfermedad\" href=\"http:\/\/omim.org\/entry\/209850?search=autism&amp;highlight=autism%20autistic\" target=\"_blank\">enfermedad del espectro autista<\/a> identific\u00f3 alteraciones en el 31 % de ellas, as\u00ed como cuatro nuevos genes candidatos de riesgo. Puede leer al respecto en <em>Jiang Y, Yuen RKC, Jin X, Wang M, Chen N, Wu X, et al. <strong><a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.cell.com\/AJHG\/fulltext\/S0002-9297%2813%2900281-4\" target=\"_blank\">Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing<\/a><\/strong>. The American Journal of Human Genetics 11 July 2013; doi:10.1016\/j.ajhg.2013.06.012<\/em>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>La secuenciaci\u00f3n del genoma completo en 32 familias con enfermedad del espectro autista identific\u00f3 alteraciones en el 31 % de ellas, as\u00ed como cuatro nuevos genes candidatos de riesgo. Puede leer al respecto en Jiang Y, Yuen RKC, Jin X, Wang M, Chen N, Wu X, et al. Detection of Clinically Relevant Genetic Variants in [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[15,25],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/1158"}],"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=1158"}],"version-history":[{"count":0,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/1158\/revisions"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=1158"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=1158"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=1158"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}