{"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":"Amniotsentees ja koorionibiopsia - Geneetika ja personaalmeditsiini kliinik","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"W2iQLaIlk3\"><a href=\"https:\/\/www.kliinikum.ee\/geneetika\/infomaterjalid-2\/amniotsentees-ja-koorionibiopsia\/\">Amniotsentees ja koorionibiopsia<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/www.kliinikum.ee\/geneetika\/infomaterjalid-2\/amniotsentees-ja-koorionibiopsia\/embed\/#?secret=W2iQLaIlk3\" width=\"600\" height=\"338\" title=\"&#8220;Amniotsentees ja koorionibiopsia&#8221; &#8212; Geneetika ja personaalmeditsiini kliinik\" data-secret=\"W2iQLaIlk3\" 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":"Lapse kromosoome on v\u00f5imalik uurida juba enne s\u00fcndi. Selline uuring v\u00f5ib osutuda vajalikuks, kui eelnevate uuringute tulemusel on j\u00e4\u00e4nud kahtlus, et tegemist v\u00f5iks olla kromosoomhaigusega. Loote kromosoomiuuring on vabatahtlik. Enne protseduuri peab pere olema n\u00f5ustatud ja teadlik, mida ja kuidas uuritakse ning andma selleks oma kirjaliku n\u00f5usoleku. Amniotsentees ehk looteveeuuring&nbsp; Sobiv aeg amniotsenteesiks ehk diagnostiliseks [&hellip;]"}