{"id":8972,"date":"2020-09-28T11:57:37","date_gmt":"2020-09-28T15:57:37","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=8972"},"modified":"2024-09-24T09:48:11","modified_gmt":"2024-09-24T13:48:11","slug":"16p12-2-deletion","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/16p12-2-deletion\/","title":{"rendered":"16p12.2 Deletion"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">The information for this summary of <\/span><strong>16p12.2 deletion syndrome<\/strong><span style=\"font-weight: 400;\"> comes from research publications. This is not meant to take the place of medical advice.<\/span><\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/16p12-2-deletion\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full 16p12.2 Deletion Gene Guide<\/strong><\/a><\/p>\n<p>The online Gene Guide includes more information about\u00a0<span class=\"notranslate\">16p11.2 deletion<\/span>\u00a0such as the chance of having another child with this condition, behavior and development concerns linked to\u00a0<span class=\"notranslate\">16p11.2 deletion<\/span>\u00a0or specialists to consider for people with this condition. Share this resource with family members or your clinical providers.<\/p>\n<p><strong><span class=\"notranslate\">16p12.2 deletion syndrome<\/span><\/strong><span style=\"font-weight: 400;\"> is also called <\/span><strong>16p12.2 microdeletion<\/strong><span style=\"font-weight: 400;\">.<\/span> <span style=\"font-weight: 400;\">For this webpage, we will be using the name <\/span><strong><span class=\"notranslate\">16p12.2 deletion syndrome<\/span><\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>The information for this summary of 16p12.2 deletion syndrome comes from research publications. This is not meant to take the place of medical advice. Click here for our full 16p12.2 Deletion Gene Guide The online Gene Guide includes more information about\u00a016p11.2 deletion\u00a0such as the chance of having another child with this condition, behavior and development [&hellip;]<\/p>\n","protected":false},"author":6,"featured_media":0,"parent":29,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-gene-card.php","meta":{"_acf_changed":false,"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"acf":[],"_links":{"self":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8972"}],"collection":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=8972"}],"version-history":[{"count":16,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8972\/revisions"}],"predecessor-version":[{"id":55266,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/8972\/revisions\/55266"}],"up":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/29"}],"wp:attachment":[{"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/media?parent=8972"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}