Figure 6From: Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalitiesExpression of candidate genes in mouse embryos. Expression levels of Trps1, Hoxc4, and Hoxc13 genes were compared among E14.5 +/+, Koa/+, and Koa/Koa embryos. Expression of Gapdh was used as a standard.Back to article page