 | Up a level |
Schroeder, Verena; Durrer, Dominik; Meili, Esther; Schubiger, Gregor; Kohler, Hans Peter (2007). Congenital factor XIII deficiency in Switzerland: from the worldwide first case in 1960 to its molecular characterisation in 2005. Swiss medical weekly, 137(19-20), pp. 272-278. EMH Media 10.4414/smw.2007.11756
Schroeder, Verena; Meili, Esther; Cung, Trinh; Schmutz, Peter; Kohler, Hans P (2006). Characterisation of six novel A-subunit mutations leading to congenital factor XIII deficiency and molecular analysis of the first diagnosed patient with this rare bleeding disorder. Thrombosis and haemostasis, 95(1), pp. 77-84. Stuttgart: Schattauer 10.1160/TH05-06-0388
