{"id":6717,"date":"2019-11-08T09:25:53","date_gmt":"2019-11-08T14:25:53","guid":{"rendered":"https:\/\/www.simonssearchlight.org\/?page_id=6717"},"modified":"2025-03-25T11:54:07","modified_gmt":"2025-03-25T15:54:07","slug":"nipbl","status":"publish","type":"page","link":"https:\/\/www.simonssearchlight.org\/research\/what-we-study\/nipbl\/","title":{"rendered":"NIPBL"},"content":{"rendered":"<p>Below is a summary for the <strong><span class=\"notranslate\">NIPBL<\/span><\/strong> gene observed in research publications. This is not meant to take the place of medical advice.<\/p>\n<p><a href=\"https:\/\/www.simonssearchlight.org\/gene-guide\/nipbl\/\" target=\"_blank\" rel=\"noopener\"><strong>Click here for our full NIPBL Gene Guide<\/strong><\/a><\/p>\n<p>The online Gene Guide includes more information about <span class=\"notranslate\">NIPBL<\/span> such as the chance of having another child with this condition, behavior and development concerns linked to <span class=\"notranslate\">NIPBL<\/span>-related syndrome or 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\">NIPBL<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> is also called<\/span> <strong>Cornelia de Lange syndrome 1<\/strong><span style=\"font-weight: 400;\">. For this webpage, we will be using the name <\/span><strong><span class=\"notranslate\">NIPBL<\/span>-related syndrome<\/strong><span style=\"font-weight: 400;\"> to encompass the wide range of variants observed in the people identified.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Genetic variants in other genes can also result in a person having <\/span><span style=\"font-weight: 400;\">Cornelia de Lange syndrome<\/span><span style=\"font-weight: 400;\">.<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Below is a summary for the NIPBL gene observed in research publications. This is not meant to take the place of medical advice. Click here for our full NIPBL Gene Guide The online Gene Guide includes more information about NIPBL such as the chance of having another child with this condition, behavior and development concerns [&hellip;]<\/p>\n","protected":false},"author":13,"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\/6717"}],"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\/13"}],"replies":[{"embeddable":true,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/comments?post=6717"}],"version-history":[{"count":11,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/6717\/revisions"}],"predecessor-version":[{"id":60714,"href":"https:\/\/www.simonssearchlight.org\/wp-json\/wp\/v2\/pages\/6717\/revisions\/60714"}],"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=6717"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}