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Site Update for Week of 12/12/2016

December 13, 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: 15q24 deletion syndrome, 16p12.2 microdeletion syndrome, Beckwith-wiedemann syndrome, BRCA1, breast-ovarian cancer, CADASIL, Chromosome 16p12.2-p11.2 deletion syndrome, Chromosome 22q11.2 duplication, chromosomes, DNA, Down syndrome, Galactosemia, Pfeiffer syndrome, Phelan-McDermid Syndrome, protein, Xeroderma pigmentosum

ThinkGenetic Joins Forces with C22C

August 30, 2016 Ruth O'Keefe 2 Comments

C22C Master Logo small

ThinkGenetic is pleased to announce the advocacy partnership with Chromosome 22 Central, Inc., also known as C22C. Chromosome 22 Central is a parent powered support organization founded in 1997 to… CONTINUE

Filed Under: News, Partners Tagged With: 22q11.2 syndrome, C22C, Cat Eye Syndrome, Chromosome 22 Central, chromosome 22 disorders, Emanuel Syndrome, genetic health, Len Barker, Mosaic Trisomy 22, Murney Rinholm, partnership, Phelan-McDermid Syndrome, Ruth O'Keefe

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