Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Lymphedema and CCBE1[original query] |
---|
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, |
Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome. American journal of medical genetics. Part A 2019 10 182 (1): 189-194. Boone Philip M, Paterson Scott, Mohajeri Kiana, Zhu Wenmiao, Genetti Casie A, Tai Derek J C, Nori Neeharika, Agrawal Pankaj B, Bacino Carlos A, Bi Weimin, Talkowski Michael E, Hogan Benjamin M, Rodan Lance |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: