-transparent.png){kind=logo}
Two new families of congenital dysfibrinogenemia originating from French Canada are reported. The dysfibrinogenemia in the first family is characterized by an abnormal aggregation of the fibrin monomers; the defect in the second family is due to a faulty release of fibrinopeptides during the proteolytic phase of the thrombin-fibrinogen reaction.
Related Publications
F Jobin, and
L Vu, and
J M Delage
May 1981,
Nederlands tijdschrift voor geneeskunde,
F Jobin, and
L Vu, and
J M Delage
June 1977,
Klinische Wochenschrift,
F Jobin, and
L Vu, and
J M Delage
July 1972,
Thrombosis et diathesis haemorrhagica,
F Jobin, and
L Vu, and
J M Delage
March 1987,
Thrombosis research,
F Jobin, and
L Vu, and
J M Delage
January 1976,
Verhandlungen der Deutschen Gesellschaft fur Innere Medizin,
F Jobin, and
L Vu, and
J M Delage
May 2012,
American journal of hematology,
F Jobin, and
L Vu, and
J M Delage
August 1975,
Klinische Wochenschrift,
F Jobin, and
L Vu, and
J M Delage
April 1983,
Thrombosis and haemostasis,
F Jobin, and
L Vu, and
J M Delage
November 1975,
Thrombosis et diathesis haemorrhagica,
F Jobin, and
L Vu, and
J M Delage
January 1980,
Annals of clinical and laboratory science,
