From germline towards somatic mutations in the pathophysiology of vascular anomaliesLIMAYE, Nisha; BOON, Laurence M; VIKKULA, Miikka et al.Human molecular genetics (Print). 2009, Vol 18, issn 0964-6906, R65-R74, NS1Article

A novel mutation in the MSX2 homeobox gene of a family with foramina parietalia permagna, headache and vascular anomalyGHASSIBE, Michella; BERNIER, Vincent; BOON, Laurence M et al.European journal of pediatrics. 2006, Vol 165, Num 10, pp 734-735, issn 0340-6199, 2 p.Article

Glomuvenous malformation (glomangioma) and venous malformation: Distinct clinicopathologic and genetic entitiesBOON, Laurence M; MULLIKEN, John B; ENJOLRAS, Odile et al.Archives of dermatology (1960). 2004, Vol 140, Num 8, pp 971-976, issn 0003-987X, 6 p.Conference Paper

A novel mutation in the SDHD gene in a family with inherited paragangliomas-implications of genetic diagnosis for follow up and treatmentRENARD, Laurette; GODFRAIND, Catherine; BOON, Laurence M et al.Head & neck. 2003, Vol 25, Num 2, pp 146-151, issn 1043-3074, 6 p.Article

Elevated D-dimer Level in the Differential Diagnosis of Venous MalformationsDOMPMARTIN, Anne; BALLIEUX, Fanny; BOON, Laurence M et al.Archives of dermatology (1960). 2009, Vol 145, Num 11, pp 1239-1244, issn 0003-987X, 6 p.Article

Congenital plaque-type glomuvenous malformations presenting in childhoodMALLORY, Susan Bayliss; ENJOLRAS, Odile; BOON, Laurence M et al.Archives of dermatology (1960). 2006, Vol 142, Num 7, pp 892-896, issn 0003-987X, 5 p.Article

Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndromePANSURIYA, Twinkal C; VAN EIJK, Ronald; WEZEL, Tom Van et al.Nature genetics. 2011, Vol 43, Num 12, pp 1256-1261, issn 1061-4036, 6 p.Article

PTHR1 mutations associated with Ollier disease result in receptor loss of functionCOUVINEAU, Alain; WOUTERS, Vinciane; BERTRAND, Guylène et al.Human molecular genetics (Print). 2008, Vol 17, Num 18, pp 2766-2775, issn 0964-6906, 10 p.Article

Mutations in a novel factor, Glomulin, are responsible for glomuvenous malformations (Glomangiomas)BROUILLARD, Pascal; BOON, Laurence M; MULLIKEN, John B et al.American journal of human genetics. 2002, Vol 70, Num 4, pp 866-874, issn 0002-9297Article

Noninvoluting congenital hemangioma: a rare cutaneous vascular anomalyENJOLRAS, Odile; MULLIKEN, John B; BOON, Laurence M et al.Plastic and reconstructive surgery (1963). 2001, Vol 107, Num 7, pp 1647-1654, issn 0032-1052Article

Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2GHALAMKARPOUR, Arash; DEBAUCHE, Christian; HAAN, Eric et al.The Journal of pediatrics. 2009, Vol 155, Num 1, pp 90-93, issn 0022-3476, 4 p.Article

Association of Localized Intravascular Coagulopathy With Venous MalformationsDOMPMARTIN, Anne; ACHER, Aurélie; VANWIJCK, Romain et al.Archives of dermatology (1960). 2008, Vol 144, Num 7, pp 873-877, issn 0003-987X, 5 p.Article

Capillary malformation-arteriovenous malformation, a new clinical and genetic disorder caused by RASH1 mutationsEEROLA, Iiro; BOON, Laurence M; MULLIKEN, John B et al.American journal of human genetics. 2003, Vol 73, Num 6, pp 1240-1249, issn 0002-9297, 10 p.Article