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Genetic Condition Update for Week of 03/06/2017

March 6, 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: ADPKD, Amyloidosis, Autosomal dominant polycystic kidney disease, BOR syndrome, Branchiootic syndrome, Branchiootorenal syndrome, Familial transthyretin amyloidosis, genetic disease, MPS IVB, Mucopolysaccharidosis type ivb, rare genetic disorder, SCADD, Short chain acyl-CoA dehydrogenase deficiency

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