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- 1997
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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
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Mark
Tubular versus conventional repair of median and ulnar nerves in the human forearm : early results from a prospective, randomized, clinical study
(
- Contribution to journal › Article
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Mark
Decreased excretion of glycosaminoglycans in patients with primary glomerular diseases
(
- Contribution to journal › Article
- 1996
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Mark
Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
(
- Contribution to journal › Article
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Mark
Computer based quantitative analysis of capillary abnormalities in systemic sclerosis and its relation to plasma concentration of von Willebrand factor
(
- Contribution to journal › Article
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Mark
Risk of malignant melanoma in relation to drug intake, alcohol, smoking and hormonal factors
(
- Contribution to journal › Article
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Mark
Reproducibility of a self-administered questionnaire for assessment of melanoma risk
(
- Contribution to journal › Article
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Mark
Familial testicular cancer in Norway and southern Sweden
(
- Contribution to journal › Article
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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
(
- Contribution to journal › Article
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Mark
Factor V:Q506 mutation and anticardiolipin antibodies in systemic lupus erythematosus
(
- Contribution to journal › Article