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ThinkGenetic to Attend and Exhibit at 13th Annual WORLDSymposium™

January 27, 2017 Ruth O'Keefe Leave a Comment

ThinkGenetic is excited to be heading to sunny San Diego, California this February to participate in the annual Lysosomal Disease Network WORLDSymposium.  The Symposium is an interdisciplinary forum to explore,… CONTINUE

Filed Under: Events Tagged With: alpha mannosidosis, Carol Ogg, Dave Jacob, Dawn Laney, diagnosis, Fabry disease, Gaucher disease, Krabbe disease, LSD, lysosomal disease, lysosomes, Morgan Simmons, Mucolipidosis, Mucopolysaccharidosis, neuronal ceroid lipfuscinosis, pompe disease, Ruth O'Keefe, Sandhoff disease, Tay-sachs disease, WORLDSymposium, WORLDSyposia

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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