Author

Geert Van Acker

Institution: Sint-Andriesziekenhuis

Observed institution: Sint-Andriesziekenhuis

OpenAlex ID: A5084625872

Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression

2011 · Gwendolyn de Bruyn, Alexandra Casaer, et al. · European Journal of Pediatrics · 20

Works count: 1

Citation count: 20

H-index: 1

I10-index: 1