J. Hinks

A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion.

J. Ingerslev, A. Goodeve, I. Peake, 2000, Blood.

A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresis

M. Makris, F. Preston, A. Goodeve, 1999, British journal of haematology.

Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor.

J. Ingerslev, A. Goodeve, I. Peake, 2000, Blood.