621 – 630 of 1919
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2018
-
Mark
FGFR3 mutation increases bladder tumourigenesis by suppressing acute inflammation
(
- Contribution to journal › Article
-
Mark
Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers
(
- Contribution to journal › Article
-
Mark
A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor
(
- Contribution to journal › Article
-
Mark
Pioneering, chromatin remodeling, and epigenetic constraint in early T-cell gene regulation by SPI1 (PU.1)
(
- Contribution to journal › Article
-
Mark
Enrichment of rare copy number variation in children with developmental language disorder
(
- Contribution to journal › Article
-
Mark
Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma
(
- Contribution to journal › Article
-
Mark
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(
- Contribution to journal › Article
-
Mark
Genetic Variants Associated with Circulating Fibroblast Growth Factor 23
(
- Contribution to journal › Article
-
Mark
Alpha 2-macroglobulin 5 bp insertion/deletion polymorphism increases the risk of recurrent venous thromboembolism
(
- Contribution to journal › Article
-
Mark
Discovering human diabetes-risk gene function with genetics and physiological assays
(
- Contribution to journal › Article