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MSH: A rare disorder of bone growth characterized by skeletal, brain, and skin abnormalities. (Genetic Home Reference[Internet]. Bethesda, MD: National Library of Medicine(US); updated 2010 June 6; cited 2010 July 9; Available from: http://ghr.nlm.nih.gov/condition=saddan/.) This disorder is associated with mutations in RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3.
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