{"version":"1.0","provider_name":"Geneetika ja personaalmeditsiini kliinik","provider_url":"https:\/\/www.kliinikum.ee\/geneetika","author_name":"K\u00fclli Kevv\u00e4i","author_url":"https:\/\/www.kliinikum.ee\/geneetika\/author\/kyllikev\/","title":"Kromosoomhaigused - Geneetika ja personaalmeditsiini kliinik","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"oZyzPgFxAO\"><a href=\"https:\/\/www.kliinikum.ee\/geneetika\/infomaterjalid-2\/kromosoomhaigused\/\">Kromosoomhaigused<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.kliinikum.ee\/geneetika\/infomaterjalid-2\/kromosoomhaigused\/embed\/#?secret=oZyzPgFxAO\" width=\"600\" height=\"338\" title=\"&#8220;Kromosoomhaigused&#8221; &#8212; Geneetika ja personaalmeditsiini kliinik\" data-secret=\"oZyzPgFxAO\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/www.kliinikum.ee\/geneetika\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","description":"Kromosoomhaigused on kromosoomianal\u00fc\u00fcsil tuvastatavad muutused kromosoomide arvus v\u00f5i ehituses. Inimese normaalseks arenguks on vajalik, et rakkudes oleks geneetilise materjali hulk tasakaalus. Kui rakud ei sisalda \u00f5iget arvu ehk 46 kromosoomi, tekitab see h\u00e4ireid normaalses arengus juba looteeast alates. Paljudel juhtudel loode hukkub enne s\u00fcndi ja rasedus katkeb iseeneslikult spontaanse abordina. Kuid v\u00f5ib ka juhtuda, et [&hellip;]"}