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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Disease and SOX18[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,
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.
International journal of cardiology 2015 Nov 204 115-121.
Costain Gregory, Lionel Anath C, Ogura Lucas, Marshall Christian R, Scherer Stephen W, Silversides Candice K, Bassett Anne
Associations of the calcium-sensing receptor gene CASR rs7652589 SNP with nephrolithiasis and secondary hyperparathyroidism in haemodialysis patients.
Scientific reports 2016 Oct 6 35188.
Grzegorzewska Alicja E, Paciorkowski Mateusz, Mostowska Adrianna, Frycz Bartosz, Warcho? Wojciech, Stolarek Ireneusz, Figlerowicz Marek, Jagodzi?ski Pawe?
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