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Genetic Condition Update for 06/02/2017

June 2, 2017 thinkgenetic Leave a Comment

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: adenosine triphosphate, ATP, bones, brittle bone disease, creatine, dienoyl coa, dienoyl-coa reductase deficiency, fracture bones, GAMT, GAMT gene, genetic neurological disorder, Guanidinoacetate methyltransferase deficiency, neurologic disorder, OI, osteogenesis imperfecta, ovarian failure, Rare Disease, rare disorder, rare genetic disease, turner syndrome

Weekly Site Update for 11/15/2016

November 11, 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: adrenal cortex, Alzheimer, Alzheimer disease, ARSA, arylsulfatase A, atrophy, Beckwith-wiedemann syndrome, Bilateral renal agenesis, biotin, biotinidase, Biotinidase deficiency, birth defects, CARASIL, Choroideremia, congenital, Congenital Adrenal Hyperplasia, Cutis Laxa, dementia, DMD, Duchenne muscular dystrophy, dystroglycanopathies, EIEE2, Epileptic encephalopathy, fetal varicella syndrome, genetic disorder, GM2, HD, Hirschsprung disease, Holocarboxylase synthetase deficiency, Huntington's disease, lactase, Lactase deficiency, metabolic condition, Metachromatic leukodystrophy, MLD, Mowat-Wilson syndrome, Mucolipidosis iii alpha, Mucolipidosis iii beta, muscle disorder, muscular dystrophy, neurologic disorder, polydystrophy, Retinitis pigmentosa, Rubinstein-Taybi syndrome, seizures, strokes, Tay-sachs disease, vision, Walker-Warburg syndrome, WWS, Xeroderma pigmentosum, XP

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