For the Focus on the NIH Undiagnosed Diseases Program
VAR-MD: A tool to analyze whole exome–genome variants in small human pedigrees with mendelian inheritance†
Version of Record online: 24 FEB 2012
© 2012 Wiley Periodicals, Inc.
Special Issue: Focus on the NIH Undiagnosed Diseases Program
Volume 33, Issue 4, pages 593–598, April 2012
How to Cite
Sincan, M., Simeonov, D. R., Adams, D., Markello, T. C., Pierson, T. M., Toro, C., Gahl, W. A. and Boerkoel, C. F. (2012), VAR-MD: A tool to analyze whole exome–genome variants in small human pedigrees with mendelian inheritance. Hum. Mutat., 33: 593–598. doi: 10.1002/humu.22034
- Issue online: 12 MAR 2012
- Version of Record online: 24 FEB 2012
- Accepted manuscript online: 30 JAN 2012 12:00AM EST
- Manuscript Accepted: 2 DEC 2011
- Manuscript Received: 12 AUG 2011
- Office of Rare Diseases Research (Dr. Stephen Groft); the NIH Clinical Center (Dr. John Gallin); and the Intramural Research Programs of the National Human Genome Research Institute and the National Institute of Neurological Disorders and Stroke
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