RDF of MGI datapubmed

S. Bruneau, et.al., 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., Developmental biology, 2001, 237
http://rdf.ncbi.nlm.nih.gov/pubmed/11543619

S. Bruneau, et.al., 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., Developmental biology, 2001, 237

pubmed

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