LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and Eye Development von Gong, Yaoqin, Slee, Roger B., Fukai, Naomi, Rawadi, Georges, Roman-Roman, Sergio, Reginato, Anthony M., Wang, Hongwei, Cundy, Tim, Glorieux, Francis H., Lev, Dorit, Zacharin, Margaret, Oexle, Konrad, Marcelino, Jose, Suwairi, Wafaa, Heeger, Shauna, Sabatakos, George, Apte, Suneel, Adkins, William N., Allgrove, Jeremy, Arslan-Kirchner, Mine, Batch, Jennifer A., Beighton, Peter, Black, Graeme C.M., Boles, Richard G., Boon, Laurence M., Borrone, Carla, Brunner, Han G., Carle, Georges F., Dallapiccola, Bruno, De Paepe, Anne, Floege, Barbara, Halfhide, Melissa Lees, Hall, Bryan, Hennekam, Raoul C., Hirose, Tatsuo, Jans, Ab, Jüppner, Harald, Kim, Chong Ae, Keppler-Noreuil, Kim, Kohlschuetter, Alfried, LaCombe, Didier, Lambert, Marie, Lemyre, Emmanuelle, Letteboer, Tom, Peltonen, Leena, Ramesar, Rajkumar S., Romanengo, Marta, Somer, Hannu, Steichen-Gersdorf, Elisabeth, Steinmann, Beat, Sullivan, Beth, Superti-Furga, Andrea, Swoboda, Walter, van den Boogaard, Marie-José, Van Hul, Wim, Vikkula, Miikka, Votruba, Marcela, Zabel, Bernhard, Garcia, Teresa, Baron, Roland, Olsen, Bjorn R., Warman, Matthew L.

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Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling von Amyere, Mustapha, Revencu, Nicole, Helaers, Raphaël, Pairet, Eleonore, Baselga, Eulalia, Cordisco, Maria, Chung, Wendy, Dubois, Josée, Lacour, Jean-Philippe, Martorell, Loreto, Mazereeuw-Hautier, Juliette, Pyeritz, Reed E, Amor, David J, Bisdorff, Annouk, Blei, Francine, Bombei, Hannah, Dompmartin, Anne, Brooks, David, Dupont, Juliette, González-Enseñat, Maria Antonia, Frieden, Ilona, Gérard, Marion, Kvarnung, Malin, Hanson-Kahn, Andrea Kwan, Hudgins, Louanne, Léauté-Labrèze, Christine, McCuaig, Catherine, Metry, Denise, Parent, Philippe, Paul, Carle, Petit, Florence, Phan, Alice, Quere, Isabelle, Salhi, Aicha, Turner, Anne, Vabres, Pierre, Vicente, Asuncion, Wargon, Orli, Watanabe, Shoji, Weibel, Lisa, Wilson, Ashley, Willing, Marcia, Mulliken, John B, Boon, Laurence M, Vikkula, Miikka

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Capillary Malformation–Arteriovenous Malformation, a New Clinical and Genetic Disorder Caused by RASA1 Mutations von Eerola, Iiro, Boon, Laurence M., Mulliken, John B., Burrows, Patricia E., Dompmartin, Anne, Watanabe, Shoji, Vanwijck, Romain, Vikkula, Miikka

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RASA1: variable phenotype with capillary and arteriovenous malformations von Boon, Laurence M, Mulliken, John B, Vikkula, Miikka

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Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”) von Brouillard, Pascal, Boon, Laurence M., Mulliken, John B., Enjolras, Odile, Ghassibé, Michella, Warman, Matthew L., Tan, O.T., Olsen, Bjorn R., Vikkula, Miikka

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Noninvoluting Congenital Hemangioma: A Rare Cutaneous Vascular Anomaly von Enjolras, Odile, Mulliken, John B, Boon, Laurence M, Wassef, Michel, Kozakewich, Harry P. W, Burrows, Patricia E

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Molecular genetics of vascular malformations von Vikkula, Miikka, Boon, Laurence M., Mulliken, John B.

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Four common glomulin mutations cause two thirds of glomuvenous malformations (“familial glomangiomas”): evidence for a founder effect von Brouillard, P, Ghassibé, M, Penington, A, Boon, L M, Dompmartin, A, Temple, I K, Cordisco, M, Adams, D, Piette, F, Harper, J I, Syed, S, Boralevi, F, Taïeb, A, Danda, S, Baselga, E, Enjolras, O, Mulliken, J B, Vikkula, M

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Complications of systemic corticosteroid therapy for problematic hemangioma von BOON, L. M, MACDONALD, D. M, MULLIKEN, J. B

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Hereditary lymphedema type I associated with VEGFR3 mutation: the first de novo case and atypical presentations von Ghalamkarpour, A, Morlot, S, Raas-Rothschild, A, Utkus, A, Mulliken, JB, Boon, LM, Vikkula, M

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Vascular Dysmorphogenesis Caused by an Activating Mutation in the Receptor Tyrosine Kinase TIE2 von Vikkula, Miikka, Boon, Laurence M, Iii, Kermit L.Carraway, Calvert, Jennifer T, Diamonti, A.John, Goumnerov, Boyan, Pasyk, Krystyna A, Marchuk, Douglas A, Warman, Matthew L, Cantley, Lewis C, Mulliken, John B, Olsen, Bjorn R

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Congenital hemangioma: Evidence of accelerated involution von Boon, Laurence M., Enjolras, Odile, Mulliken, John B.

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KRIT1 is mutated in hyperkeratotic cutaneous capillary-venous malformation associated with cerebral capillary malformation von Eerola, I, Plate, K H, Spiegel, R, Boon, L M, Mulliken, J B, Vikkula, M

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A Gene for Inherited Cutaneous Venous Anomalies (“Glomangiomas”) Localizes to Chromosome 1p21-22 von Boon, Laurence M., Brouillard, Pascal, Irrthum, Alexandre, Karttunen, Leena, Warman, Matthew L., Rudolph, Ross, Mulliken, John B., Olsen, Bjorn R., Vikkula, Miikka

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Locus for susceptibility for familial capillary malformation (‘port-wine stain’) maps to 5q von Eerola, Iiro, Boon, Laurence M, Watanabe, Shoji, Grynberg, Henri, Mulliken, John B, Vikkula, Miikka

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Hepatic vascular anomalies in infancy: A twenty-seven-year experience von Boon, Laurence M., Burrows, Patricia E., Paltiel, Harriet J., Lund, Dennis P., Ezekowitz, R.Alan B., Folkman, Judah, Mulliken, John B.

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Glomuvenous Malformation (Glomangioma) and Venous Malformation: Distinct Clinicopathologic and Genetic Entities von Boon, Laurence M, Mulliken, John B, Enjolras, Odile, Vikkula, Miikka

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A novel mutation in the SDHD gene in a family with inherited paragangliomas-implications of genetic diagnosis for follow up and treatment von Renard, Laurette, Godfraind, Catherine, Boon, Laurence M., Vikkula, Miikka

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Dysbacteriosis and squamous (pre)neoplasia of immigrants and Dutch women as established in population-based cervical screening von Verbruggen, Banut-Sabine M., Boon, Mathilde E., Boon, L. Matthijs

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E-selectin is present in proliferating endothelial cells in human hemangiomas von Kraling, BM, Razon, MJ, Boon, LM, Zurakowski, D, Seachord, C, Darveau, RP, Mulliken, JB, Corless, CL, Bischoff, J

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