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Taking a Closer Look at Advocacy- The SynGAP1 Research Fund

January 11, 2022 Jessica Dronen, MS, CGC Leave a Comment

Collaboration, Transparency, Urgency ThinkGenetic is honored to partner with many incredible organizations, each with their own stories, struggles and triumphs. This month, we are taking a moment to highlight the… CONTINUE

Filed Under: Advocacy, Advocacy Alliance, Partners Tagged With: Advocacy Alliance, Dawn Laney, Mike Graglia, SYNGAP, SynGAP Research Fund, SYNGAP1

Site Update for Week of 12/01/2016

December 1, 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 anyone searching for answers on genetic diseases and… CONTINUE

Filed Under: Updates Tagged With: Acromegaly, Acyl-coa dehydrogenase, ADAMTSL4, Agammaglobulinemia, Alagille syndrome, Alkaptonuria, Campomelic dysplasia, Cartilage-hair hypoplasia, Ceroid lipofuscinosis, CHARGE syndrome, chromosome pairs, congenital heart defect, developmental delay, DNA, enzyme, Fabry, Gal-1-PUT, galactose-1-phosphate uridyl transferase, Galactosemia, gene, genetic condition, glucose, Glutaric acidemia, glycogen storage disease, growth hormone, Huntington, hypogonadotropic hypogonadism, Kallman syndrome, Leopard syndrome, Mosaic trisomy 14, Noonan syndrome, Otosclerosis, Pitt-Hopkins syndrome, pituitary gland, protein, PTHS, Rare Disease, rare genetic disorder, Rett syndrome, Robinow syndrome, Sandhoff disease, Sickle cell anemia, Spinal muscular atrophy, Stickler syndrome, sugar, SYNGAP1, triple X syndrome, Trisomy 13, Trisomy x, webbed neck, XXX

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

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