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Human Molecular Genetics|April 30, 2003
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeBenjamin M Kriederman, Teressa L Myloyde, Marlys H Witte, et al.
Frontiers in Physiology|October 30, 2024
Cancer and lymphatic marker FOXC2 drives wound healing and fibrotic tissue formationMaia B Granoski, Katharina S Fischer, William W Hahn, et al.
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