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The Canadian Organization for Rare Disorders (CORD) is a Canadian registered charity that is a network of organizations who represent people affected by rare diseases.CORD's purpose is to provide a strong common voice advocating for a healthcare system and health policy for those with rare disorders.
CTV Nature Channel was licensed by the Canadian Radio-television and Telecommunications Commission (CRTC) on December 14, 2000 as Discovery Civilization Channel Canada. [2] The application was granted to CTV Inc., and was later transferred to its subsidiary, CTV Specialty Television Inc., in which ESPN owns a 20% interest.
Harvard College v Canada (Commissioner of Patents) [2] is a leading Supreme Court of Canada case concerning the patentability of higher life forms within the context of the Patent Act. [3] At issue was the patentability of the Harvard oncomouse , a mouse that had its genome genetically altered by a cancer-promoting gene ( oncogene ).
Research at CMMT is focused on discovering genetic susceptibility to illnesses such as Huntington Disease, Type 2 diabetes and bipolar disorder. In 2008, the founder of CMMT, Dr. Michael Hayden , was named "Researcher of the Year" by the Canada Institutes of Health Research. [ 1 ]
Bipartisan bills introduced in Congress Thursday would effectively ban a Chinese genomics firm from doing business in America. Intel officials have warned China is grabbing U.S. genetic info.
The Genetic Non-Discrimination Act (French: Loi sur la non-discrimination génétique) of 2017, also known as Bill S-201 during the 2nd Session of the 41st Parliament of Canada and the 1st Session of the 42nd Parliament of Canada, originated in a Private Member's Bill. [1] [2] It was introduced by Senators James Cowan [3] and Jennifer O'Connell ...
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DNA Family Secrets is a British television series which began airing on BBC Two in March 2021. [1] The programme is presented by Stacey Dooley and geneticist, Professor Turi King, and uses the latest DNA technology to solve family mysteries around ancestry, missing relatives and genetic disease.
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