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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.Journal of the American Academy of Dermatology|January 22, 2000
Residual lesions after Kasabach-Merritt phenomenon in 41 patientsO Enjolras, J B Mulliken, M Wassef, et al.The Journal of Burn Care & Rehabilitation|November 1, 1989
Healing characteristics of expanded autografts on wounds covered with homograft and Biobrane temporary wound dressingC E Hartford, X W Wang, V M Peterson, et al.Cell|November 5, 1993
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosisE W Jabs, U Müller, X Li, et al.AJNR. American Journal of Neuroradiology|July 24, 2010
Klippel-Trenaunay syndrome and spinal arteriovenous malformations: an erroneous associationA I Alomari, D B Orbach, J B Mulliken, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 20, 1999
Human NELL-1 expressed in unilateral coronal synostosisK Ting, H Vastardis, J B Mulliken, et al.American Journal of Human Genetics|August 1, 1995
Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational familiesJ Stein, J B Mulliken, S Stal, 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.Pageof 21