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- 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
- Contribution to journal › Letter
-
Mark
Relation of alleles of the collagen type Ialpha1 gene to bone density and the risk of osteoporotic fractures in postmenopausal women
- Contribution to journal › Article
- 1997
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Mark
Phenotypes and genotypes in families with hereditary tapetoretinal degenerations
(1997)
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic and phenotypic analysis of a large (122-member) protein S-deficient kindred provides an explanation for the familial coexistence of type I and type III plasma phenotypes
- Contribution to journal › Article
-
Mark
Activated protein C resistance caused by a common factor V mutation has a single origin
- Contribution to journal › Article
-
Mark
Evaluation of original and modified APC-resistance tests in unselected outpatients with clinically suspected thrombosis and in healthy controls
- Contribution to journal › Article
-
Mark
Polymorphisms of the interleukin-6 gene are associated with bone mineral density
- Contribution to journal › Article
- 1996
-
Mark
HLA-DQB1*0201/0302 is associated with severe retinopathy in patients with IDDM
- Contribution to journal › Article
-
Mark
Activated protein C resistance as a basis for venous thrombosis.
- Contribution to journal › Article
- 1995
-
Mark
Hepatitis C superinfection in hepatitis C virus (HCV)-infected patients transplanted with an HCV-infected kidney
- Contribution to journal › Article
