Communicating new knowledge on previously reported genetic variants
Open Access
- 1 August 2012
- journal article
- Published by Elsevier in Genetics in Medicine
- Vol. 14 (8), 713-719
- https://doi.org/10.1038/gim.2012.19
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Making a definitive diagnosis: Successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel diseaseGenetics in Medicine, 2011
- Initial impact of the sequencing of the human genomeNature, 2011
- The GeneInsight suite: a platform to support laboratory and provider use of DNA-based genetic testingHuman Mutation, 2011
- Use and interpretation of genetic tests in cardiovascular geneticsHeart, 2010
- Multidimensional Results Reporting to Participants in Genomic Studies: Getting It RightScience Translational Medicine, 2010
- ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007Genetics in Medicine, 2008
- Duty to re-contactGenetics in Medicine, 1999