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  Scientists have made further discoveries into the genetics of antithrombin deficiency, which places some individuals at a raised risk of clotting disorders. Hereditary deficiency in antithrombin affects about one in two thousan...
1 month ago
  A new genetic syndrome caused by biallelic mutations in the Fanconi anaemia complementation group M (FANCM) gene predisposes the body to cancer, new research has discovered. Research led by Jordi Surrallés, professor of the Dep...
1 month ago