Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression
Year: 2011
Type: article
Study design: Case Report
Source: European Journal of Pediatrics
Authors: Gwendolyn de Bruyn, Alexandra Casaer, Katrien Devolder, Geert Van Acker, Hilde Logghe, Koen Devriendt, Luc Cornette
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2137836655