{"id":805,"date":"2014-03-26T17:49:35","date_gmt":"2014-03-26T22:49:35","guid":{"rendered":"http:\/\/sciencemediacentre.ca\/site\/?p=805"},"modified":"2014-04-04T12:59:12","modified_gmt":"2014-04-04T17:59:12","slug":"questions-sur-le-depistage-chez-les-nouveaux-nes-a-laide-du-sequencage-du-genome-entier","status":"publish","type":"post","link":"http:\/\/sciencemediacentre.ca\/site\/questions-sur-le-depistage-chez-les-nouveaux-nes-a-laide-du-sequencage-du-genome-entier\/","title":{"rendered":"Questions sur le d\u00e9pistage chez les nouveaux-n\u00e9s \u00e0 l&#8217;aide du s\u00e9quen\u00e7age du g\u00e9nome entier<img src=\"http:\/\/sciencemediacentre.ca\/site\/wp-content\/uploads\/2014\/01\/canada_flag_icon_small.gif\">"},"content":{"rendered":"<div id=\"attachment_803\" style=\"width: 367px\" class=\"wp-caption aligncenter\"><a href=\"http:\/\/sciencemediacentre.ca\/site\/wp-content\/uploads\/2014\/04\/446px-Karyotype.png\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-803\" class=\" wp-image-803 \" alt=\"Les m\u00e9decins peuvent examiner le g\u00e9nome d'un nouveau-n\u00e9 afin de d\u00e9terminer si l'enfant peut souffrir des maladies g\u00e9n\u00e9tiques connues dans l'avenir. (Cr\u00e9dit photo: National Human Genome Research Institute, Wikimedia commons)\" src=\"http:\/\/sciencemediacentre.ca\/site\/wp-content\/uploads\/2014\/04\/446px-Karyotype.png\" width=\"357\" height=\"384\" srcset=\"http:\/\/sciencemediacentre.ca\/site\/wp-content\/uploads\/2014\/04\/446px-Karyotype.png 446w, http:\/\/sciencemediacentre.ca\/site\/wp-content\/uploads\/2014\/04\/446px-Karyotype-278x300.png 278w\" sizes=\"auto, (max-width: 357px) 100vw, 357px\" \/><\/a><p id=\"caption-attachment-803\" class=\"wp-caption-text\">Les m\u00e9decins peuvent examiner le g\u00e9nome d&#8217;un nouveau-n\u00e9 afin de d\u00e9terminer si l&#8217;enfant peut souffrir des maladies g\u00e9n\u00e9tiques connues dans l&#8217;avenir. (Cr\u00e9dit photo: National Human Genome Research Institute, <a href=\"http:\/\/commons.wikimedia.org\/wiki\/File:Karyotype.png\" target=\"_blank\">Wikimedia commons<\/a>)<\/p><\/div>\n<p>Le d\u00e9pistage des nouveaux n\u00e9s peut maintenant utiliser les avanc\u00e9es du s\u00e9quen\u00e7age du g\u00e9nome entier pour d\u00e9tecter des maladies g\u00e9n\u00e9tiques, endocriniennes ou m\u00e9taboliques pr\u00e9coces. Dans un commentaire, des auteurs de l\u2019Universit\u00e9 McGill dressent une liste de questions \u00e9thiques, l\u00e9gales et sociales sur le futur du d\u00e9pistage des nouveaux-n\u00e9s. Ils estiment que l\u2019int\u00e9r\u00eat des enfants doit passer avant tout avant d\u2019apporter toute modification aux programmes de d\u00e9pistage universel.<\/p>\n<p><!--more--><\/p>\n<p>Pour lire l\u2019article original publi\u00e9 dans<em>\u00a0Science Translational Medicine<\/em>\u00a0le\u00a0<strong>26 mars 2014<\/strong>,\u00a0<span style=\"text-decoration: underline;\"><a href=\"http:\/\/stm.sciencemag.org\/content\/6\/229\/229cm2.full?sid=5c4a35d1-e674-4ff3-8c23-1279f1cf9c4e\" target=\"_blank\">cliquez\u00a0ici<\/a><\/span>.<\/p>\n<p><span style=\"text-decoration: underline;\"><strong>Auteur \u00e0 contacter pour plus d\u2019informations<\/strong><\/span><\/p>\n<h4><a href=\"http:\/\/www.genomicsandpolicy.org\/en\/team-member\/no9\" target=\"_blank\"> Bartha Knoppers<\/a>, Universit\u00e9 McGill<\/h4>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Le d\u00e9pistage des nouveaux n\u00e9s peut maintenant utiliser les avanc\u00e9es du s\u00e9quen\u00e7age du g\u00e9nome entier pour d\u00e9tecter des maladies g\u00e9n\u00e9tiques, endocriniennes ou m\u00e9taboliques pr\u00e9coces. Dans un commentaire, des auteurs de l\u2019Universit\u00e9 McGill dressent une liste de questions \u00e9thiques, l\u00e9gales et sociales sur le futur du d\u00e9pistage des nouveaux-n\u00e9s. Ils estiment que l\u2019int\u00e9r\u00eat des enfants doit [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":803,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[531],"tags":[910,694,842,695],"class_list":["post-805","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-paper-of-interest-fr","tag-genetique","tag-medecine","tag-quebec","tag-sante"],"jetpack_featured_media_url":"http:\/\/sciencemediacentre.ca\/site\/wp-content\/uploads\/2014\/04\/446px-Karyotype.png","jetpack_shortlink":"https:\/\/wp.me\/p4DqbN-cZ","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/posts\/805","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/comments?post=805"}],"version-history":[{"count":1,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/posts\/805\/revisions"}],"predecessor-version":[{"id":806,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/posts\/805\/revisions\/806"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/media\/803"}],"wp:attachment":[{"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/media?parent=805"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/categories?post=805"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/sciencemediacentre.ca\/site\/wp-json\/wp\/v2\/tags?post=805"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}