Hämostaseologie, Inhaltsverzeichnis Hamostaseologie 2019; 39(S 01): S1-S92DOI: 10.1055/s-0039-1680156 SY20 Rare Bleeding Disorders Georg Thieme Verlag KG Stuttgart · New YorkCorrelation of Genotype and Phenotype in Congenital FXI Deficiency Autoren Institutsangaben A. Banchev 1 Institute for Experimental Haematology and Transfusion Medicine, University Bonn, Molecular Haemostasilogy, Bonn, Germany B. Pezeshkpoor 1 Institute for Experimental Haematology and Transfusion Medicine, University Bonn, Molecular Haemostasilogy, Bonn, Germany B. Preisler 1 Institute for Experimental Haematology and Transfusion Medicine, University Bonn, Molecular Haemostasilogy, Bonn, Germany A. Stupar 1 Institute for Experimental Haematology and Transfusion Medicine, University Bonn, Molecular Haemostasilogy, Bonn, Germany A. Pavlova 2 Institute for Experimental Haematology and Transfusion Medicine, University Bonn, Bonn, Germany J. Oldenburg 1 Institute for Experimental Haematology and Transfusion Medicine, University Bonn, Molecular Haemostasilogy, Bonn, Germany Artikel empfehlen Abstract Volltext
