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

N.T. Bech-Hansen

Department of Medical Genetics

University of Calgary

Alberta

Canada

[email]@acs.ucalgary.ca

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, University of Calgary, Alberta, Canada. 1998

References

  1. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Bech-Hansen, N.T., Naylor, M.J., Maybaum, T.A., Pearce, W.G., Koop, B., Fishman, G.A., Mets, M., Musarella, M.A., Boycott, K.M. Nat. Genet. (1998) [Pubmed]
  2. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23. Bech-Hansen, N.T., Boycott, K.M., Gratton, K.J., Ross, D.A., Field, L.L., Pearce, W.G. Hum. Genet. (1998) [Pubmed]
 
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