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	1.	No CCM2 mutations in a cohort of 31 sporadic cases. [electronic resource] by Verlaan, D J Laurent, S B Rouleau, G A Siegel, A M Producer: 20050804 In: Neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Large germline deletions and duplication in isolated cerebral cavernous malformation patients. [electronic resource] by Felbor, U Gaetzner, S Verlaan, D J Vijzelaar, R Rouleau, G A Siegel, A M Producer: 20080123 In: Neurogenetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cerebral cavernous malformations: mutations in Krit1. [electronic resource] by Verlaan, D J Davenport, W J Stefan, H Sure, U Siegel, A M Rouleau, G A Producer: 20020522 In: Neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	CCM3 mutations are uncommon in cerebral cavernous malformations. [electronic resource] by Verlaan, D J Roussel, J Laurent, S B Elger, C E Siegel, A M Rouleau, G A Producer: 20060414 In: Neurology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	CCM1 mutation screen of sporadic cases with cerebral cavernous malformations. [electronic resource] by Verlaan, D J Laurent, S B Sure, U Bertalanffy, H Andermann, E Andermann, F Rouleau, G A Siegel, A M Producer: 20040802 In: Neurology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3. [electronic resource] by Verlaan, D J Dubé, M-P St-Onge, J Noreau, A Roussel, J Satgé, N Wallace, M C Rouleau, G A Producer: 20060630 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families. [electronic resource] by Graeni, C Stepper, F Sturzenegger, M Merlo, A Verlaan, D J Andermann, F Baumann, C R Bonassin, F Georgiadis, D Baumgartner, R W Rouleau, G A Siegel, A M Producer: 20100402 In: Neurosurgical review vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families]. [electronic resource] by Siegel, A M Bertalanffy, H Dichgans, J J Elger, C E Hopf, H Hopf, N Keidel, M Kleider, A Nowak, G Pfeiffer, R A Schramm, J Spuck, S Stefan, H Sure, U Baumann, C R Rouleau, G A Verlaan, D J Andermann, E Andermann, F Producer: 20050927 In: Der Nervenarzt vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study. [electronic resource] by Richards, J B Rivadeneira, F Inouye, M Pastinen, T M Soranzo, N Wilson, S G Andrew, T Falchi, M Gwilliam, R Ahmadi, K R Valdes, A M Arp, P Whittaker, P Verlaan, D J Jhamai, M Kumanduri, V Moorhouse, M van Meurs, J B Hofman, A Pols, H A P Hart, D Zhai, G Kato, B S Mullin, B H Zhang, F Deloukas, P Uitterlinden, A G Spector, T D Producer: 20080515 In: Lancet (London, England) vol. 371 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)