{"id":57515,"date":"2012-11-12T17:50:05","date_gmt":"2012-11-12T17:50:05","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/genetics-center-takes-part-in-global-meet.php"},"modified":"2012-11-12T17:50:05","modified_gmt":"2012-11-12T17:50:05","slug":"genetics-center-takes-part-in-global-meet","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/human-genetics\/genetics-center-takes-part-in-global-meet.php","title":{"rendered":"Genetics Center takes part in global meet"},"content":{"rendered":"<p><p>Four researchers from the Shafallah Medical          Genetics Center (SMGC) have participated in an          international human genetics meeting in San Francisco,          California, USA to present the findings of their research          projects in Qatar.          The meeting is the 62nd annual meeting of the American          Society of Human Genetics. It was held between November          6-10. It is the largest human genetics meeting and          exposition in the world. It attracted about 7,000          scientific attendees and more than 200 exhibiting          companies. American Society of Human Genetics members and          leading scientists from around the world are selected to          present their research findings at invited platform or          poster sessions, during a 5 day packed programme. In          addition, exhibitors show state-of-the-art medical and          laboratory equipment, products, services and computer          software designed to enhance human genetics research,          teaching and diagnostics.          The four researchers presented five posters that reflect          on the research activities they had performed at SMGC in          Doha. Two posters reported on gene discovery in two rare          genetic conditions. One condition is found in one Qatari          family and is related to mental retardation and multiple          birth defects. The other condition represents a skin          disease associated with a kidney defect with abnormal          skin and low potassium levels in the blood of patients. A          third poster reflects on the advances in bioinformatics          tools that were adopted by SMGC to analyse large sets of          genomic data. Two posters identify novel mutations in          previously described genes and their relation to specific          genetic disorders.          Hassan Ali bin Ali, the chairman of the Shafallah Center,          said: The researchers contribution to and participation          at the American Society of Human Genetics meeting          demonstrated the SMGC is now a world class genetics          center that not only serves and helps the children at          Shafallah, but contributes to the advancement of          scientific knowledge on a global basis. The staff work          very hard and it is encouraging to know that their          research produces meaningful and positive          outcomes.<\/p>\n<\/p>\n<p>Read more: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.gulf-times.com\/site\/topics\/article.asp?cu_no=2&amp;item_no=543236&amp;version=1&amp;template_id=36&amp;parent_id=16\" title=\"Genetics Center takes part in global meet\">Genetics Center takes part in global meet<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Four researchers from the Shafallah Medical Genetics Center (SMGC) have participated in an international human genetics meeting in San Francisco, California, USA to present the findings of their research projects in Qatar. The meeting is the 62nd annual meeting of the American Society of Human Genetics <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/human-genetics\/genetics-center-takes-part-in-global-meet.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[4],"tags":[],"class_list":["post-57515","post","type-post","status-publish","format-standard","hentry","category-human-genetics"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/57515"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=57515"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/57515\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=57515"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=57515"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=57515"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}