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	1.	Patients' and their family members' understanding of the genetics of type 1 von Willebrand disease. [electronic resource] by Lanke, E Lanke, J Lethagen, S Producer: 20081210 In: Haemophilia : the official journal of the World Federation of Hemophilia vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic analysis of 31 Swedish type 1 von Willebrand disease families reveals incomplete linkage to the von Willebrand factor gene and a high frequency of a certain disease haplotype. [electronic resource] by Lanke, E Johansson, A M Halldén, C Lethagen, S Producer: 20060221 In: Journal of thrombosis and haemostasis : JTH vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1. [electronic resource] by Lanke, E Johansson, A M Hillarp, A Lethagen, S Zöller, B Dahlbäck, B Halldén, C Producer: 20050517 In: Journal of thrombosis and haemostasis : JTH vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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