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- 1998
-
Mark
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
(
- Contribution to journal › Article
-
Mark
Heterogeneity of the blood group Ax allele: genetic recombination of common alleles can result in the Ax phenotype
(
- Contribution to journal › Article
-
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]
(
- Contribution to journal › Letter
-
Mark
A common 4G allele in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene as a risk factor for pulmonary embolism and arterial thrombosis in hereditary protein S deficiency
(
- Contribution to journal › Article
- 1997
-
Mark
Molecular Genetic Studies of the Blood Group ABO Locus in Man
1997)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
(
- Contribution to journal › Article
- 1996
-
Mark
HLA-DQB1*0201/0302 is associated with severe retinopathy in patients with IDDM
(
- Contribution to journal › Article
-
Mark
High prevalence of the FVR506Q mutation causing APC resistance in a region of southern Sweden with a high incidence of venous thrombosis.
(
- Contribution to journal › Letter
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