Small bowel obstruction secondary to atheromatous embolism. A case report and review of the literature.

Por Mulliken, J B, Bartlett, M K
Publicado em 1971

Cervicofacial Venous Malformations: MRI Features and Interventional Strategies

Por Konez, O., Burrows, P. E., Mulliken, J.B.
Publicado em 2002

Twenty year experience in maxillocraniofacial surgery. An evaluation of early surgery on growth, function and body image.

Por Murray, J E, Mulliken, J B, Kaban, L B, Belfer, M
Publicado em 1979

Use of demineralized allogeneic bone implants for the correction of maxillocraniofacial deformities.

Por Mulliken, J B, Glowacki, J, Kaban, L B, Folkman, J, Murray, J E
Publicado em 1981

Propranolol Targets Contractility of Infantile Hemangioma-derived Pericytes

Por Lee, D., Boscolo, E., Durham, J.T., Mulliken, J.B., Herman, I.M., Bischoff, J.
Publicado em 2014

Further Evidence Suggesting a Role for Variation in ARHGAP29 in Nonsyndromic Cleft Lip/Palate

Por Letra, A., Maili, L., Mulliken, J.B., Buchanan, E., Blanton, S.H., Hecht, J.T.
Publicado no Birth Defects Res A Clin Mol Teratol (2014)

Cerebrofacial Venous Anomalies, Sinus Pericranii, Ocular Abnormalities and Developmental Delay

Por Macit, B., Burrows, P.E., Yilmaz, S., Orbach, D.B., Mulliken, J.B., Alomari, A.I.
Publicado em 2012

Cellular markers that distinguish the phases of hemangioma during infancy and childhood.

Por Takahashi, K, Mulliken, J B, Kozakewich, H P, Rogers, R A, Folkman, J, Ezekowitz, R A
Publicado em 1994

Nonsyndromic cleft lip with or without cleft palate: evidence of linkage to BCL3 in 17 multigenerational families.

Por Stein, J, Mulliken, J B, Stal, S, Gasser, D L, Malcolm, S, Winter, R, Blanton, S H, Amos, C, Seemanova, E, Hecht, J T
Publicado em 1995

Nonsyndromic cleft lip with or without cleft palate: erratum.

Por Amos, C., Stein, J., Mulliken, J. B., Stal, S., Malcolm, S., Winter, R., Blanton, S. H., Seemanova, E., Gasser, D. L., Hecht, J. T.
Publicado em 1996

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

Mutation Analysis of Core Binding Factor A1 in Patients with Cleidocranial Dysplasia

Por Quack, I., Vonderstrass, B., Stock, M., Aylsworth, A. S., Becker, A., Brueton, L., Lee, P. J., Majewski, F., Mulliken, J. B., Suri, M., Zenker, M., Mundlos, S., Otto, F.
Publicado em 1999

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

A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome

Por Muenke, M., Gripp, K. W., McDonald-McGinn, D. M., Gaudenz, K., Whitaker, L. A., Bartlett, S. P., Markowitz, R. I., Robin, N. H., Nwokoro, N., Mulvihill, J. J., Losken, H. W., Mulliken, J. B., Guttmacher, A. E., Wilroy, R. S., Clarke, L. A., Hollway, G., Adès, L. C., Haan, E. A., Mulley, J. C., Cohen, M. M., Bellus, G. A., Francomano, C. A., Moloney, D. M., Wall, S. A., Wilkie, A. O. M., Zackai, E. H.
Publicado em 1997