DOI:
10.1055/s-00033990
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References
Lanke E, Johansson AM, Halldén C, Lethagen S.
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.
J Thromb Haemost 2005;
3 (12) 2656-2663
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