We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleFOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.AuthorsKriederman BM; Myloyde TL; Witte MH; Dagenais SL; Witte CL; Rennels M; Bernas MJ; Lynch MT; Erickson RP; Caulder MS; Miura N; Jackson D; Brooks BP; Glover TWPublicationHuman molecular genetics, 2003, Vol 12, Issue 10, p1179ISSN0964-6906Publication typearticleDOI10.1093/hmg/ddg123