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Allele Publication :

Type  Used-FC Publication . Mgi Jnum  J:134490
Publication . Citation  Raz R, et al. (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 syndrome. Development 135(9):1713-23
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