{"id":4357,"date":"2018-06-08T18:50:59","date_gmt":"2018-06-08T16:50:59","guid":{"rendered":"https:\/\/f101g.org\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\/"},"modified":"2018-06-08T18:50:59","modified_gmt":"2018-06-08T16:50:59","slug":"de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot","status":"publish","type":"post","link":"https:\/\/f101g.org\/nl\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\/","title":{"rendered":"\u201eDe F101G vult een leemte in de ondersteuning van genetisch onderzoek\u201d door C\u00e9cile Chabot"},"content":{"rendered":"<p><strong>1. Kunt u zich alstublieft voorstellen?<\/strong><\/p>\n<p style=\"text-align: justify;\">Mijn naam is C\u00e9cile Chabot. Ik heb het syndroom van Marfan. Ik nam deel aan de activiteiten van de ABSM en richtte deze vereniging op met andere directeuren. Ik ben vooral ge\u00efnteresseerd in de F101G vanwege de hoop die het ons geeft op het gebied van fundamenteel onderzoek.<\/p>\n<p style=\"text-align: justify;\"><strong>2. Waarom steunt u het 101 Genomes Marfan Project?<\/strong><\/p>\n<p style=\"text-align: justify;\">Een van de grootste problemen bij Marfan is namelijk de variabiliteit in de expressie van de ziekte. Dit is nog steeds een echte onbekende voor ons: waarom sommige mensen meer last hebben van het syndroom en andere minder. Ik zie fundamenteel genetisch onderzoek als een manier om antwoorden te geven op de vraag naar variatie in de expressie van ziekten.<\/p>\n<p style=\"text-align: justify;\"><strong>3. Wat verwacht je als iemand met het Marfan syndroom van het 101 Genomes Project?<\/strong><\/p>\n<p style=\"text-align: justify;\">Mijn hoop is tweeledig&nbsp;Op persoonlijk niveau, om uit te zoeken of dit de mensen die mij volgen kan helpen om hun zorgstrategie\u00ebn op de lange termijn te verfijnen, maar ook, meer in het algemeen, met betrekking tot andere mensen met de ziekte van Marfan, om bijvoorbeeld, als ik zelf deelnam aan de teststeekproef, te kunnen helpen de ziekte beter te begrijpen en hen te helpen meer geschikte, meer gerichte zorg te krijgen.  <u>Concluderend, voor mij vult de F101G een leemte die nog steeds bestaat, namelijk ondersteuning voor genetisch onderzoek, en dat vind ik bijzonder belangrijk<\/u>.<\/p>\n<p style=\"text-align: right;\"><strong>C\u00e9cile Chabot, DES Europees recht,<br \/>\nMaster in de rechten, Jurist.<\/strong><\/p>\n<p>&nbsp;<\/p>\n<p>[embedyt]  https:\/\/www.youtube.com\/watch?v=kNIKuTa_UXk[\/embedyt]<\/p>\n<p>&nbsp;<\/p>\n<p>[embedyt]  https:\/\/www.youtube.com\/watch?v=kdW2a4IvJgU[\/embedyt]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>1. Kunt u zich alstublieft voorstellen? Mijn naam is C\u00e9cile Chabot. Ik heb het syndroom van Marfan. Ik nam deel &hellip;<\/p>\n","protected":false},"author":3,"featured_media":2689,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2}},"categories":[120],"tags":[81,82],"class_list":["post-4357","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-capsule-nl","tag-marfan-nl","tag-patient-nl"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>&quot;De F101G vult een leemte in de ondersteuning van genetisch onderzoek&quot; door C\u00e9cile Chabot%page%-101 Genomes Foundation - Genomics voor zeldzame ziekten<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/f101g.org\/nl\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\/\" \/>\n<meta property=\"og:locale\" content=\"nl_BE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"&quot;De F101G vult een leemte in de ondersteuning van genetisch onderzoek&quot; door C\u00e9cile Chabot%page%-101 Genomes Foundation - Genomics voor zeldzame ziekten\" \/>\n<meta property=\"og:description\" content=\"1. Kunt u zich alstublieft voorstellen? Mijn naam is C\u00e9cile Chabot. Ik heb het syndroom van Marfan. Ik nam deel &hellip;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/f101g.org\/nl\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\/\" \/>\n<meta property=\"og:site_name\" content=\"101 Genomes Foundation - Genomics voor zeldzame ziekten\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/F101Genomes\" \/>\n<meta property=\"article:published_time\" content=\"2018-06-08T16:50:59+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/f101g.org\/wp-content\/uploads\/2018\/06\/12-Cecile-Chabot.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"692\" \/>\n\t<meta property=\"og:image:height\" content=\"562\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/jpeg\" \/>\n<meta name=\"author\" content=\"Ludivine Verboogen\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Geschreven door\" \/>\n\t<meta name=\"twitter:data1\" content=\"Ludivine Verboogen\" \/>\n\t<meta name=\"twitter:label2\" content=\"Geschatte leestijd\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minuut\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\\\/\"},\"author\":{\"name\":\"Ludivine Verboogen\",\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/#\\\/schema\\\/person\\\/62f6469b30eae292c8f15f99dd41c064\"},\"headline\":\"\u201eDe F101G vult een leemte in de ondersteuning van genetisch onderzoek\u201d door C\u00e9cile Chabot\",\"datePublished\":\"2018-06-08T16:50:59+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\\\/\"},\"wordCount\":285,\"publisher\":{\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/f101g.org\\\/wp-content\\\/uploads\\\/2018\\\/06\\\/12-Cecile-Chabot.jpg\",\"keywords\":[\"Marfan\",\"Pati\u00ebnt\"],\"articleSection\":[\"Capsule\"],\"inLanguage\":\"nl-BE\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/f101g.org\\\/nl\\\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\\\/\",\"url\":\"https:\\\/\\\/f101g.org\\\/nl\\\/de-f101g-vult-een-leemte-in-de-ondersteuning-van-genetisch-onderzoek-door-cecile-chabot\\\/\",\"name\":\"\\\"De F101G vult een leemte in de ondersteuning van genetisch onderzoek\\\" door C\u00e9cile Chabot%page%-101 Genomes Foundation - 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