FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome

Benjamin M. Kriederman, Teressa L. Myloyde, Marlys H. Witte, Susan L. Dagenais, Charles L. Witte, Margaret Rennels, Michael J. Bernas, Michelle T. Lynch, Robert P. Erickson, Mark S. Caulder, Naoyuki Miura, David Jackson, Brian P. Brooks, Thomas W. Glover

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