{"id":3158,"date":"2016-07-05T12:38:38","date_gmt":"2016-07-05T12:38:38","guid":{"rendered":"http:\/\/blogs.sld.cu\/oserranob\/?p=3158"},"modified":"2016-07-06T19:11:05","modified_gmt":"2016-07-06T19:11:05","slug":"utilidad-de-pruebas-para-hipoacusia","status":"publish","type":"post","link":"https:\/\/blogs.sld.cu\/oserranob\/2016\/07\/05\/utilidad-de-pruebas-para-hipoacusia\/","title":{"rendered":"Utilidad de pruebas para hipoacusia"},"content":{"rendered":"<p style=\"text-align: justify\"><a href=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2016\/07\/Hearing.jpg\"><img loading=\"lazy\" class=\"alignleft size-thumbnail wp-image-3233\" style=\"border-width: 1px;margin: 5px\" src=\"https:\/\/blogs.sld.cu\/oserranob\/files\/2016\/07\/Hearing-150x123.jpg\" alt=\"Hearing\" width=\"85\" height=\"70\" \/><\/a>Dos art\u00edculos tratan sobre el diagn\u00f3stico gen\u00e9tico y gen\u00f3mico de los trastornos auditivos:<br \/>\n&#8211; Wu CC, Tsai CH, Hung CC, Lin YH, Lin YH, Huang FL, <em>et al<\/em>. <a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.nature.com\/gim\/journal\/vaop\/ncurrent\/full\/gim201666a.html\" target=\"_blank\">Newborn genetic screening for hearing impairment: a population-based longitudinal study<\/a>. Genetics in Medicine 2016; doi:10.1038\/gim.2016.66.<br \/>\n&#8211; Abou Tayoun AN, Al Turki SH, Oza AM, Bowser MJ, Hernandez AL, Funke BH, <em>et al<\/em>. <a title=\"Texto completo en ingl\u00e9s\" href=\"http:\/\/www.nature.com\/gim\/journal\/v18\/n6\/full\/gim2015141a.html\" target=\"_blank\">Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing\u2013based diagnostic testing and interpretation<\/a>. Genetics in Medicine 2016;18(6):545\u2013553.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Dos art\u00edculos tratan sobre el diagn\u00f3stico gen\u00e9tico y gen\u00f3mico de los trastornos auditivos: &#8211; Wu CC, Tsai CH, Hung CC, Lin YH, Lin YH, Huang FL, et al. Newborn genetic screening for hearing impairment: a population-based longitudinal study. Genetics in Medicine 2016; doi:10.1038\/gim.2016.66. &#8211; Abou Tayoun AN, Al Turki SH, Oza AM, Bowser MJ, Hernandez [&hellip;]<\/p>\n","protected":false},"author":125,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[14,15,21],"tags":[],"_links":{"self":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3158"}],"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=3158"}],"version-history":[{"count":3,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3158\/revisions"}],"predecessor-version":[{"id":3235,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/posts\/3158\/revisions\/3235"}],"wp:attachment":[{"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/media?parent=3158"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/categories?post=3158"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.sld.cu\/oserranob\/wp-json\/wp\/v2\/tags?post=3158"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}