1 – 7 of 7
- show: 50
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2017
-
Mark
Expanded national database collection and data coverage in the FINDbase worldwide database for clinically relevant genomic variation allele frequencies
(
- Contribution to journal › Article
- 2012
-
Mark
VarioML framework for comprehensive variation data representation and exchange
(
- Contribution to journal › Article
-
Mark
Human variome project country nodes: Documenting genetic information within a country
(
- Contribution to journal › Article
- 2011
-
Mark
Clarity and claims in variation/mutation databasing.
(
- Contribution to journal › Letter
- 2009
-
Mark
Capturing all disease-causing mutations for clinical and research use: toward an effortless system for the Human Variome Project.
(
- Contribution to journal › Article
-
Mark
Planning the human variome project: the Spain report.
(
- Contribution to journal › Article
- 2007
-
Mark
PhenCode: connecting ENCODE data with mutations and phenotype.
(
- Contribution to journal › Article