11 – 13 of 13
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=""
width=""
height=""
allowtransparency="true"
frameborder="0">
</iframe>
- « previous
- 1
- 2
- next »
- 1998
-
Mark
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families [3]
Zöller, Bengt LU
; Svensson, P.J.
LU
; Dahlbäck, Björn
LU
and Hillarp, A.
LU
(1998)
In Blood
91(6).
p.2210-2211
- Contribution to journal › Letter
- 1997
-
Mark
The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
Hillarp, Andreas LU ; Zöller, Bengt LU
; Svensson, Peter
LU
and Dahlbäck, Björn
LU
(1997)
In Thrombosis and Haemostasis
78(3).
p.2-990
- Contribution to journal › Debate/Note/Editorial
- 1996
-
Mark
Elevated levels of prothrombin activation fragment 1 + 2 in plasma from patients with heterozygous Arg506 to Gln mutation in the factor V gene (APC-resistance) and/or inherited protein S deficiency
Zöller, Bengt LU
; Holm, Johan
LU
; Svensson, Peter
LU
and Dahlbäck, B
LU
(1996)
In Thrombosis and Haemostasis
75(2).
p.270-274
- Contribution to journal › Article
- « previous
- 1
- 2
- next »