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Genetic Condition Update for Week of 03/31/2017

March 31, 2017 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: Fetal parvovirus, Hereditary hemorrhagic telangiectasia, HHT, Long-chain 3-hydroxyacyl-coa dehydrogenase deficiency, Lynch syndrome, Phenylketonuria, ThinkGenetic, tyrosinemia type 1, update

Weekly Site Update for 08/29/2016

August 29, 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 disease… CONTINUE

Filed Under: Updates Tagged With: 22q11.2, 22q11.2 deletion syndrome, CAMRQ1, Cerebellar ataxia, CMV, Cytomegalovirus, DHMN5, Distal hereditary motor neuropathy, dysequilibrium syndrome, Fetal cytomegalovirus, glycogen storage disease, GSD1a, Hypophosphatasia, LCHADD, Long-chain 3-hydroxyacyl-coa dehydrogenase deficiency, mental retardation, TAT, Tyrosinemia, VLDLR

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