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Proceedings of the National Academy of Sciences of the United States of America|May 8, 2008
A soluble activin type IIA receptor induces bone formation and improves skeletal integrityR Scott Pearsall, Ernesto Canalis, Milton Cornwall-Brady, et al.Development (Cambridge, England)|March 21, 2008
The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndromeRegina Raz, Sigmar Stricker, Elizabetta Gazzerro, et al.Pageof 2