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Hydrops fetalis and pulmonary lymphangiectasia due toFOXC2mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression

✍ Scribed by Gwendolyn de Bruyn; Alexandra Casaer; Katrien Devolder; Geert Van Acker; Hilde Logghe; Koen Devriendt; Luc Cornette


Book ID
106122382
Publisher
Springer
Year
2011
Tongue
English
Weight
304 KB
Volume
171
Category
Article
ISSN
0340-6997

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