Benjamin M. Kriederman, et.al., FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome., Human molecular genetics, 2003, 12
Benjamin M. Kriederman, et.al., FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome., Human molecular genetics, 2003, 12