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 |