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(1 - 4 of 4)
Clinical Interpretation of Variants from Next-Generation Sequencing: The 2016 Scientific Meeting of the Human Genome Variation Society
Oetting, W.S.; Brookes, A.J.; Beroud, C.; Taschner, P.E. 2016
Clinical Interpretation of Variants from Next-Generation Sequencing: The 2016 Scientific Meeting of the Human Genome Variation Society
Article / Letter to editor
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Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation Society
Oetting, W.S.; Brenner, S.E.; Brookes, A.J.; Greenblatt, M.S.; Hart, R.K.; Karchin, R.; ... ; Taschner, P.E. 2016
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation Society
Article / Letter to editor
metadata only
Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting
Kalman, L.V.; Agundez, J.A.G.; Appell, M.L.; Black, J.L.; Bell, G.C.; Boukouvala, S.; ... ; Zanger, U.M. 2016
Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting
Article / Letter to editor
metadata only
Getting Ready for the Human Phenome Project: The 2012 Forum of the Human Variome Project
Oetting, W.S.; Robinson, P.N.; Greenblatt, M.S.; Cotton, R.G.; Beck, T.; Carey, J.C.; ... ; Zhao, E.Y. 2013
Getting Ready for the Human Phenome Project: The 2012 Forum of the Human Variome Project
Article / Letter to editor
metadata only