HuGE Literature Finder
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Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Molecular syndromology 2013 Sep 4 (6): 257-66. Mendola A, Schlögel M J, Ghalamkarpour A, Irrthum A, Nguyen H L, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken J B, Boon L M, Brouillard P, Vikkula M, |
Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment. Clinical cancer research : an official journal of the American Association for Cancer Research 2012 Apr 18 (8): 2382-90. Finegold David N, Baty Catherine J, Knickelbein Kelly Z, Perschke Shelley, Noon Sarah E, Campbell Diana, Karlsson Jenny M, Huang Diana, Kimak Mark A, Lawrence Elizabeth C, Feingold Eleanor, Meriney Stephen D, Brufsky Adam M, Ferrell Robert |
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- Page last updated:Mar 31, 2023
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