Milroy disease and the VEGFR-3 mutation phenotype.
Brice, G.; Child, A. H.; Evans, A.; Bell, R.; Mansour, S.; Bumand, K.; Sarfarazi, M.; Jeffery, S.; Mortimer, P.; Journal of Medical Genetics, 2005, vol. 42, issue 2, p 98, ISSN 00222593. ISBN 14686244.

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