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508433
508433
http://dx.doi.org/10.1086/508433
A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome
P356
Q24672101-F015C66A-7636-45D1-92DF-75198168EE43
P356
508433
http://dx.doi.org/10.1086/508433