Contract grant sponsors: FORGE (Finding Of Rare disease GEnes) Canada Consortium; Canadian Institutes of Health Research; Ontario Genomics Institute (OGI-049); Genome Quebec; Genome British Columbia; McLaughlin Centre; CIHR Catalyst grant; Ontario MEDI Genomes2Life grant.
PhenoTips: Patient Phenotyping Software for Clinical and Research Use
Article first published online: 24 MAY 2013
© 2013 WILEY PERIODICALS, INC.
Volume 34, Issue 8, pages 1057–1065, August 2013
How to Cite
Girdea, M., Dumitriu, S., Fiume, M., Bowdin, S., Boycott, K. M., Chénier, S., Chitayat, D., Faghfoury, H., Meyn, M. S., Ray, P. N., So, J., Stavropoulos, D. J. and Brudno, M. (2013), PhenoTips: Patient Phenotyping Software for Clinical and Research Use. Hum. Mutat., 34: 1057–1065. doi: 10.1002/humu.22347
Communicated by Peter N. Robinson
- Issue published online: 15 JUL 2013
- Article first published online: 24 MAY 2013
- Accepted manuscript online: 1 MAY 2013 10:46AM EST
- Manuscript Accepted: 18 APR 2013
- Manuscript Received: 18 JAN 2013
- FORGE (Finding Of Rare disease GEnes) Canada Consortium
- Canadian Institutes of Health Research
- Ontario Genomics Institute. Grant Number: OGI-049
- Genome Quebec
- Genome British Columbia
- McLaughlin Centre
- CIHR Catalyst
- Ontario MEDI Genomes2Life
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