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- 1999
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Mark
Thrombophilia as a multigenic disease
(
- Contribution to journal › Article
- 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
Extracellular ATP: a growth factor for vascular smooth muscle cells
(
- Contribution to journal › Scientific review
-
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
-
Mark
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect
(
- Contribution to journal › Article
-
Mark
MEN1 gene mutations in 12 MEN1 families and their associated tumors
(
- Contribution to journal › Article
-
Mark
Creatine kinase knockout mice - what is the phenotype : Skeletal muscle
(
- Contribution to journal › Article
- 1997
-
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
- 1996
-
Mark
PDGF-A signaling is a critical event in lung alveolar myofibroblast development and alveogenesis.
(
- Contribution to journal › Article