Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
Nature Genetics2000Vol. 24(3), pp. 275–278
Citations Over TimeTop 1% of 2000 papers
Michael Oldridge, Ana María Fortuna, Monika Maringa, Peter Propping, Sahar Mansour, C. Pollitt, Thomas M. DeChiara, Robert B. Kimble, David M. Valenzuela, George D. Yancopoulos, Andrew O.M. Wilkie
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