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Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiencyPINTAO, Maria C; GARCIA, A. A; BORGEL, D et al.Human genetics. 2009, Vol 126, Num 3, pp 449-456, issn 0340-6717, 8 p.Article

A reduced sensitivity for activated protein C in the absence of factor V Leiden increases the risk of venous thrombosisDE VISSER, M. C. H; ROSENDAAL, F. R; BERTINA, R. M et al.Blood. 1999, Vol 93, Num 4, pp 1271-1276, issn 0006-4971Article

The HR2 haplotype of factor V : Effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosisDE VISSER, M. C. H; GUASCH, J. F; KAMPHUISEN, P. W et al.Thrombosis and haemostasis. 2000, Vol 83, Num 4, pp 577-582, issn 0340-6245Article

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