Associated Papers
Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.
de Bruyn G et al.
European Journal of Pediatrics, 2012
Lymphedema-distichiasis syndrome and FOXC2 gene mutation.
Traboulsi EI et al.
American Journal of Ophthalmology, 2002
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