{"id":4136,"date":"2018-04-22T02:14:08","date_gmt":"2018-04-22T02:14:08","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=4136"},"modified":"2018-04-26T04:42:14","modified_gmt":"2018-04-26T04:42:14","slug":"variaciones-en-estudios-de-brca12-para-cancer-de-mama-y-ovario","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2018\/04\/22\/variaciones-en-estudios-de-brca12-para-cancer-de-mama-y-ovario\/","title":{"rendered":"Variaciones en estudios de BRCA1\/2 para c\u00e1ncer de mama y ovario"},"content":{"rendered":"<p style=\"text-align: justify\"><a href=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2018\/04\/2018-04-25-BRCA.jpg\"><img loading=\"lazy\" class=\"alignleft wp-image-4177 size-full\" style=\"border-width: 1px;margin: 5px\" title=\"(c) Toland AE, et al. npj Genomic Medicine 2018.\" src=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2018\/04\/2018-04-25-BRCA.jpg\" alt=\"2018 04 25 BRCA\" width=\"100\" height=\"86\" \/><\/a>Una encuesta a 86 laboratorios del mundo ha revelado que el 93 % utiliza la secuenciaci\u00f3n masiva paralela en la pesquisa de las mutaciones de los genes <a title=\"Informaci\u00f3n sobre el gen en Gene\" href=\"https:\/\/www.ncbi.nlm.nih.gov\/gene\/672\" target=\"_blank\">BRCA1<\/a> y <a title=\"Informaci\u00f3n sobre el gen en Gene\" href=\"https:\/\/www.ncbi.nlm.nih.gov\/gene\/675\" target=\"_blank\">BRCA2<\/a> para las formas hereditarias de los tumores malignos de <a title=\"Informaci\u00f3n sobre la enfermedad en OMIM\" href=\"http:\/\/omim.org\/entry\/114480\" target=\"_blank\">mama<\/a> y <a title=\"Informaci\u00f3n sobre la enfermedad en OMIM\" href=\"http:\/\/omim.org\/entry\/167000\" target=\"_blank\">ovario<\/a>. Puede leer otros resultados en Toland AE, Forman A, Couch FJ, Culver JO, Eccles DM, Foulkes WD, <em>et al<\/em>. <a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.nature.com\/articles\/s41525-018-0046-7\" target=\"_blank\">Clinical testing of BRCA1 and BRCA2: a worldwide snapshot of technological practices<\/a>. npj Genomic Medicine 2018;3:7.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Una encuesta a 86 laboratorios del mundo ha revelado que el 93 % utiliza la secuenciaci\u00f3n masiva paralela en la pesquisa de las mutaciones de los genes BRCA1 y BRCA2 para las formas hereditarias de los tumores malignos de mama y ovario. Puede leer otros resultados en Toland AE, Forman A, Couch FJ, Culver JO, [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[37,11,15],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4136"}],"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=4136"}],"version-history":[{"count":3,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4136\/revisions"}],"predecessor-version":[{"id":4179,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/4136\/revisions\/4179"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=4136"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=4136"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=4136"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}