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Weekly Site Update for 10/03/2016

October 3, 2016 thinkgenetic Leave a Comment

recently added updates

ThinkGenetic strives to create, update and review content regularly to ensure the information we provide is accurate, referenced and available 24/7 to our audience. If you wish to see your… CONTINUE

Filed Under: Updates Tagged With: achondrogensis, Alpha-thalassemia, Andersen-Tawil Syndome, attention deficits, birth defects, Cardiofaciocutaneous syndrome, Congenital insensitivity to pain, cysts, Duchenne and becker muscular dystrophy, Familial adenomatous polyposis, GM2, hemangioblastomas, Hemophilia A, Hemophilia B, Hypophosphatasia, Lysosomal acid lipase deficiency, mood disorders, neurological, Phenylketonuria, Prader-willi syndrome, Roberts syndrome, Sotos syndrome, SYNGAP1, Tay-Sachs, tumors, VHL, Von Hippel-Lindau

Protected: UK-Based PolyPeople Joins ThinkGenetic in Raising Awareness of Rare Cancers

March 28, 2016 Ruth O'Keefe Leave a Comment

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Filed Under: Partners Tagged With: advocacy partnership, Familial adenomatous polyposis, FAP, PolyPeople, rare cancer, support group, ThinkGenetic

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