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Primary lymphedema
- ... Karkkainen MJ, Devriendt K, Alitalo K, Vikkula M. Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase. Am J Hum Genet. 2000 Aug;67(2):295-301. doi: 10.1086/303019. Epub 2000 ... with VEGFR-3 signalling in primary lymphoedema. Nat Genet. 2000 Jun;25(2):153- ...
- ... of the eye area and lymphatic vessels, the primary regions of the body affected by lymphedema-distichiasis syndrome. More About This Health Condition FKHL14 ...