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Cell|December 27, 1996
Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2M Vikkula, L M Boon, K L Carraway, et al.Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.The British Journal of Dermatology|October 8, 2017
Development of an international core outcome set for peripheral vascular malformations: the OVAMA projectS E R Horbach, C M A M van der Horst, F Blei, et al.Journal of Medical Genetics|February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effectP Brouillard, M Ghassibé, A Penington, et al.Molecular Syndromology|June 27, 2013
Genotypes and phenotypes of 162 families with a glomulin mutationP Brouillard, L M Boon, N Revencu, et al.Molecular Syndromology|June 27, 2013
Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb OvergrowthN Revencu, L M Boon, A Dompmartin, et al.Cell|November 24, 2001
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye developmentY Gong, R B Slee, N Fukai, et al.Pageof 4