Hämostaseologie, Inhaltsverzeichnis Hamostaseologie 2024; 44(S 01): S60DOI: 10.1055/s-0044-1779150 Abstracts Topics T-08. Other congenital bleeding disorders Impact of Next Generation Sequencing on molecular genetic analysis in patients with multiple coagulation factor deficiencies Authors Institutsangaben B. Preisler 1 University Clinic Bonn, Institute of Experimental Hematology and Transfusion Medicine, Bonn, Germany B. Pezeshkpoor 1 University Clinic Bonn, Institute of Experimental Hematology and Transfusion Medicine, Bonn, Germany R. Fischer 2 SRH Kurpfalzkrankenhaus Heidelberg, Hemophilia Care Center, Heidelberg, Germany A. Pavlova 1 University Clinic Bonn, Institute of Experimental Hematology and Transfusion Medicine, Bonn, Germany J. Oldenburg 1 University Clinic Bonn, Institute of Experimental Hematology and Transfusion Medicine, Bonn, Germany Artikel empfehlen Abstract Volltext Referenzen References 1 Ver Donck F, Downes K, Freson K.. Strengths and limitations of high-throughput sequencing for the diagnosis of inherited bleeding and platelet disorders. J Thromb Haemost 2020; 18: 1839-1845 2 Preisler B., Pezeshkpoor B., Banchev A., Fischer R., Zieger B., Scholz U., Rühl H., Kemkes-Matthes B., Schmitt U., Redlich A.. et al. Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients—A Single-Center Experience in Genetic Diagnosis. J. Clin. Med. 2021; 10: 347
