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European Journal of Gynaecological Oncology|November 16, 2005
Koilocytosis and squamous (pre)neoplasia as detected in population-based cervical screening: practice and theoryM E Boon, L M Boon, M J A de Bosschere, et al.The Journal of Pediatrics|September 1, 1996
Hepatic vascular anomalies in infancy: a twenty-seven-year experienceL M Boon, P E Burrows, H J Paltiel, et al.American Journal of Human Genetics|June 12, 1999
A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22L M Boon, P Brouillard, A Irrthum, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 30, 2019
A not so harmless mass: Kaposiform hemangioendothelioma complicated by a Kasabach-Merritt phenomenonS Tribolet, C Hoyoux, L M Boon, et al.European Journal of Human Genetics : EJHG|February 15, 2001
Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YACA Irrthum, P Brouillard, O Enjolras, et al.The American Journal of Pathology|April 1, 1996
E-selectin is present in proliferating endothelial cells in human hemangiomasB M Kräling, M J Razon, L M Boon, et al.AJNR. American Journal of Neuroradiology|December 17, 2009
A novel association between RASA1 mutations and spinal arteriovenous anomaliesR Thiex, J B Mulliken, N Revencu, et al.Journal of Medical Genetics|March 1, 1995
A gene for familial venous malformations maps to chromosome 9p in a second large kindredC J Gallione, K A Pasyk, L M Boon, et al.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.Pageof 4