Publications by authors named "Geert Van Acker"

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Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.
Gwendolyn de Bruyn, Alexandra Casaer, Katrien Devolder, Geert Van Acker, Hilde Logghe

Eur J Pediatrยท March 2012

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