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- 2004
-
Mark
Haplotype Structure and Genotype-Phenotype Correlations of the Sulfonylurea Receptor and the Islet ATP-Sensitive Potassium Channel Gene Region.
(
- Contribution to journal › Article
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Mark
Heritability of ambulatory and office blood pressure phenotypes in Swedish families.
(
- Contribution to journal › Article
- 2003
-
Mark
A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Scan in Families With Maturity-Onset Diabetes of the Young: Evidence for Further Genetic Heterogeneity.
(
- Contribution to journal › Article
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
(
- Contribution to journal › Article
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Mark
Pro-opiomelanocortin gene is associated with serum leptin levels in lean but not in obese individuals.
(
- Contribution to journal › Article
- 2002
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
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Mark
A variation in 3 ' UTR of hPTP1B increases specific gene expression and associates with insulin resistance
(
- Contribution to journal › Article
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Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
(
- Contribution to journal › Article
- 2001
-
Mark
The metabolic syndrome influences the risk of chronic complications in patients with type II diabetes
(
- Contribution to journal › Article