Aytac, S. Et Al. 2010. Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon. HAEMOPHILIA , vol.16, no.2 , 408.

Aytac, S., ÜNAL, S., Coskun, T., Tokatli, A., Sivri, S., DURSUN, A., ... Cila, A.(2010). Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon. HAEMOPHILIA , vol.16, no.2, 408.

Aytac, S. Et Al. "Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon," HAEMOPHILIA , vol.16, no.2, 408, 2010

Aytac, S. Et Al. "Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon." HAEMOPHILIA , vol.16, no.2, pp.408, 2010

Aytac, S. Et Al. (2010) . "Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon." HAEMOPHILIA , vol.16, no.2, p.408.

@article{article, author={S. Aytac Et Al. }, title={Von Willebrand disease associated with heterozygous factor V G1691A mutation and thrombosis in a patient with mut(0) methylmalonic acidemia: a paradoxical phenomenon}, journal={HAEMOPHILIA}, year=2010, pages={408} }