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Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B
2000
232 citations
Journal Article
Field-Weighted Citation Impact:
14.28
Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B | Researchclopedia
Regeneron (United States)
Robert B. Kimble
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Regeneron (United States)
David M. Valenzuela
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Regeneron (United States)
George D. Yancopoulos
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Regeneron (United States)
Andrew O.M. Wilkie
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John Radcliffe Hospital