Xla Wt + cdknx MO nf2 has 1 phenotype(s)
Images Sources Experiment + Assay Phenotypes Human Diseases
FIG. 4B

Naylor RW et al. (2009) 		Xla Wt + cdknx MO nf2

NF22 (in situ hybridization)
Expression Phenotype
absent lhx1.L expression in pronephric mesenchyme