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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

R.B. Lowry

Department of Medical Genetics

Alberta Children's Hospital and University of Calgary

Calgary

Alberta

Canada

[email]@crha-health.ab.ca

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, Alberta Children's Hospital and University of Calgary, Calgary, Alberta, Canada. 2001

References

  1. Syndrome of coronal craniosynostosis, Klippel-Feil anomaly, and sprengel shoulder with and without Pro250Arg mutation in the FGFR3 gene. Lowry, R.B., Jabs, E.W., Graham, G.E., Gerritsen, J., Fleming, J. Am. J. Med. Genet. (2001) [Pubmed]
 
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