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Allele Publication :

Type  Used-FC Publication . Mgi Jnum  J:71694
Publication . Citation  Bruneau S, et al. (2001) The mouse hoxd13(spdh) mutation, a polyalanine expansion similar to human type ii synpolydactyly (spd), disrupts the function but not the expression of other hoxd genes. Dev Biol 237(2):345-53
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