Variable Somatic TIE2 Mutations in Half of Sporadic Venous Malformations

Por Soblet, J., Limaye, N., Uebelhoer, M., Boon, L.M., Vikkula, M.
Publicado em 2013

A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

Por Boon, L M, Brouillard, P, Irrthum, A, Karttunen, L, Warman, M L, Rudolph, R, Mulliken, J B, Olsen, B R, Vikkula, M
Publicado em 1999

E-selectin is present in proliferating endothelial cells in human hemangiomas.

Por Kräling, B. M., Razon, M. J., Boon, L. M., Zurakowski, D., Seachord, C., Darveau, R. P., Mulliken, J. B., Corless, C. L., Bischoff, J.
Publicado em 1996

A gene for familial venous malformations maps to chromosome 9p in a second large kindred.

Por Gallione, C J, Pasyk, K A, Boon, L M, Lennon, F, Johnson, D W, Helmbold, E A, Markel, D S, Vikkula, M, Mulliken, J B, Warman, M L
Publicado em 1995

Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

Por 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.
Publicado em 2013

Genotypes and Phenotypes of 162 Families with a Glomulin Mutation

Por Brouillard, P., Boon, L.M., Revencu, N., Berg, J., Dompmartin, A., Dubois, J., Garzon, M., Holden, S., Kangesu, L., Labrèze, C., Lynch, S.A., McKeown, C., Meskauskas, R., Quere, I., Syed, S., Vabres, P., Wassef, M., Mulliken, J.B., Vikkula, M.
Publicado em 2013

Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth

Por Revencu, N., Boon, L.M., Dompmartin, A., Rieu, P., Busch, W.L., Dubois, J., Forzano, F., van Hagen, J.M., Halbach, S., Kuechler, A., Lachmeijer, A.M.A., Lähde, J., Russell, L., Simola, K.O.J., Mulliken, J.B., Vikkula, M.
Publicado em 2013