Authors: de Visser, MCH Poort, SR Vos, HL Rosendaal, FR Bertina, RM

Citation: Mch. De Visser et al., Factor X levels, polymorphisms in the promoter region of factor X, and therisk of venous thrombosis, THROMB HAEM, 85(6), 2001, pp. 1011-1017

Authors: Garcia, EBG Poort, SR Stibbe, J Sturk, A Schaap, MCL Kappers, M Bertina, RM

Citation: Ebg. Garcia et al., Two novel and one recurrent missense mutation in the factor XIII A gene intwo Dutch patients with factor XIII deficiency, BR J HAEM, 112(2), 2001, pp. 513-518

Authors: Strijks, E Poort, SR Renier, WO Gabreels, FJM Bertina, RM

Citation: E. Strijks et al., Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy. (vol 30, pg 320, 1999), NEUROPEDIAT, 31(4), 2000, pp. 223-223

Authors: Strijks, E Poort, SR Renier, WO Gabreels, FJM Bertina, RM

Citation: E. Strijks et al., Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy, NEUROPEDIAT, 30(6), 1999, pp. 320-324

Authors: Poort, SR Njo, KT Vos, HL Bertina, RM

Citation: Sr. Poort et al., Two novel mutations in the prothrombin gene cause severe bleeding in a compound heterozygous patient, BL COAG FIB, 9(8), 1998, pp. 761-764