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Citation: M. Wylenzek et al., A novel point mutation in the 3 ' region of the prothrombin gene at position 20221 in a Lebanese/Syrian family, THROMB HAEM, 85(5), 2001, pp. 943-944

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Citation: Jde. Van Suijlen et al., Multicentre evaluation of the Boehringer Mannheim/Hitachi 917 analysis system, J AUTOM M M, 22(3), 2000, pp. 65-81

Authors: Klingler, KR Zech, D Wielckens, K

Citation: Kr. Klingler et al., Haemochromatosis: Automated detection of the two point mutations in the HFE gene: Cys282Tyr and His63Asp, CLIN CH L M, 38(12), 2000, pp. 1225-1230

Authors: Wiebe, C Holzem, G Wielckens, K Klingler, KR

Citation: C. Wiebe et al., Apolipoprotein E polymorphism: Automated determination of apolipoprotein E2, E3, and E4 isoforms, LIPIDS, 35(1), 2000, pp. 99-104

Authors: Klingler, KR Grote, S Holzem, G Wielckens, K

Citation: Kr. Klingler et al., Activated protein C (APC)-resistance: Automated detection of the point mutation at position 1691 in the factor V gene, CLIN CH L M, 37(2), 1999, pp. 101-107

Authors: Klingler, KR Junold, T Wielckens, K

Citation: Kr. Klingler et al., Activated protein C resistance: Automated detection of the factor V Leidenmutation by mismatch hybridization, CLIN CHEM, 45(11), 1999, pp. 1925-1931