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

Partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification

Por Douglas, J, Tatton-Brown, K, Coleman, K, Guerrero, S, Berg, J, Cole, T, FitzPatrick, D, Gillerot, Y, Hughes, H, Pilz, D, Raymond, F, Temple, I, Irrthum, A, Schouten, J, Rahman, N
Publicado em 2005

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

The AURORA initiative for metastatic breast cancer

Por Zardavas, D, Maetens, M, Irrthum, A, Goulioti, T, Engelen, K, Fumagalli, D, Salgado, R, Aftimos, P, Saini, K S, Sotiriou, C, Campbell, P, Dinh, P, von Minckwitz, G, Gelber, R D, Dowsett, M, Di Leo, A, Cameron, D, Baselga, J, Gnant, M, Goldhirsch, A, Norton, L, Piccart, M
Publicado no Br J Cancer (2014)

Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome

Por Tatton-Brown, K, Douglas, J, Coleman, K, Baujat, G, Chandler, K, Clarke, A, Collins, A, Davies, S, Faravelli, F, Firth, H, Garrett, C, Hughes, H, Kerr, B, Liebelt, J, Reardon, W, Schaefer, G, Splitt, M, Temple, I, Waggoner, D, Weaver, D, Wilson, L, Cole, T, Cormier-Daire, V, Irrthum, A, Rahman, N, on, b
Publicado em 2005