{"id":4183,"date":"2019-03-15T20:51:05","date_gmt":"2019-03-15T19:51:05","guid":{"rendered":"https:\/\/f101g.org\/annual-meeting-of-the-belgian-society-of-human-genetics\/"},"modified":"2019-03-15T20:51:05","modified_gmt":"2019-03-15T19:51:05","slug":"annual-meeting-of-the-belgian-society-of-human-genetics","status":"publish","type":"post","link":"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/","title":{"rendered":"Annual meeting of the Belgian Society of Human Genetics"},"content":{"rendered":"<p><em><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-761 alignleft\" src=\"https:\/\/f101g.org\/wp-content\/uploads\/2019\/03\/20190315-Photo-02.jpg\" alt=\"\" width=\"373\" height=\"281\">On March 15, 2019, the <sup>19th<\/sup> annual meeting of the Belgian Society of Human Genetics (BeSHG) took place at the Palais des Congr\u00e8s in Li\u00e8ge. Romain was invited to close this annual meeting by presenting to all Belgian geneticists the work of the 101 Genomes Foundation in general and the 101 Genomes Project dedicated to Marfan syndrome in particular.<\/em>.<\/p>\n<p>At the invitation of Professors Gert Matthijs and Vincent Bours, Romain closed the annual meeting of the Belgian Society of Human Genetics<a href=\"#_ftn1\" name=\"_ftnref1\">[1]<\/a>, which this year was devoted to precision medicine&nbsp;: &#8221;&nbsp;<em>Precision Medicine: Application of Genetics in Prevention and Treatment<\/em>&nbsp;&#8220;.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-760 alignright\" src=\"https:\/\/f101g.org\/wp-content\/uploads\/2019\/03\/20190315-Photo-01-e1765977455172.jpg\" alt=\"\" width=\"373\" height=\"280\">The presentation was very well received. Representatives of several genetics centers have expressed their willingness to take part in the F101G adventure, and even to contribute directly to the pilot 101 Genomes Project dedicated to Marfan syndrome.<\/p>\n<p>Addressing all the genetics professionals gathered at their annual <em>barnum<\/em> was a difficult exercise. But it was also a real honor to be able to instill in the minds of these healthcare professionals the importance of making the diagnosis of Marfan syndrome as quickly as possible.<\/p>\n<p><a href=\"#_ftnref1\" name=\"_ftn1\">[1]<\/a> &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;  To find out more about BeSHG, visit&nbsp;: http: <a href=\"http:\/\/www.beshg.be\/\">\/\/www.beshg.be\/<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-759\" src=\"https:\/\/f101g.org\/wp-content\/uploads\/2019\/03\/20190315-BeSHG-Affiche.png\" alt=\"\" width=\"488\" height=\"603\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>On March 15, 2019, the 19th annual meeting of the Belgian Society of Human Genetics (BeSHG) took place at the &hellip;<\/p>\n","protected":false},"author":3,"featured_media":2795,"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":[172],"tags":[91],"class_list":["post-4183","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-event","tag-scientist"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v26.9 - 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Genomics for Rare Diseases\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/F101Genomes\" \/>\n<meta property=\"article:published_time\" content=\"2019-03-15T19:51:05+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/f101g.org\/wp-content\/uploads\/2019\/03\/20190315-Photo-01-1024x768.jpg\" \/>\n\t<meta property=\"og:image:width\" content=\"1024\" \/>\n\t<meta property=\"og:image:height\" content=\"768\" \/>\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=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Ludivine Verboogen\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/#article\",\"isPartOf\":{\"@id\":\"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/\"},\"author\":{\"name\":\"Ludivine Verboogen\",\"@id\":\"https:\/\/f101g.org\/en\/#\/schema\/person\/62f6469b30eae292c8f15f99dd41c064\"},\"headline\":\"Annual meeting of the Belgian Society of Human Genetics\",\"datePublished\":\"2019-03-15T19:51:05+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/\"},\"wordCount\":208,\"publisher\":{\"@id\":\"https:\/\/f101g.org\/en\/#organization\"},\"image\":{\"@id\":\"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/#primaryimage\"},\"thumbnailUrl\":\"https:\/\/f101g.org\/wp-content\/uploads\/2019\/03\/20190315-Photo-01-e1765977669886.jpg\",\"keywords\":[\"Scientist\"],\"articleSection\":[\"Event\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/\",\"url\":\"https:\/\/f101g.org\/en\/annual-meeting-of-the-belgian-society-of-human-genetics\/\",\"name\":\"Annual meeting of the Belgian Society of Human Genetics - 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