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

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Hilary Vallance

Department of Pathology and Laboratory Medicine

University of British Columbia

Vancouver

Canada V6H 3N1

[email]@cw.bc.ca

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada V6H 3N1. 2006
  • Biochemical Genetics Laboratory, Department of Pathology and Laboratory Medicine, Children's and Women's Health Centre of British Columbia, Vancouver, Canada. 2003 - 2004
  • Department of Pathology, Children's and Women's Health Centre of British Columbia, 4500 Oak Street, Room 2F22, Canada. 2004

References

  1. Common HEXB polymorphisms reduce serum HexA and HexB enzymatic activities, potentially masking Tay-Sachs disease carrier identification. Vallance, H., Morris, T.J., Coulter-Mackie, M., Lim-Steele, J., Kaback, M. Mol. Genet. Metab. (2006) [Pubmed]
  2. Pseudo-lysosomal storage disease caused by EMLA cream. Vallance, H., Chaba, T., Clarke, L., Taylor, G. J. Inherit. Metab. Dis. (2004) [Pubmed]
  3. Biochemical approach to the investigation of pediatric mitochondrial disease. Vallance, H. Pediatr. Dev. Pathol. (2004) [Pubmed]
  4. Carrier testing for autosomal-recessive disorders. Vallance, H., Ford, J. Crit. Rev. Clin. Lab. Sci (2003) [Pubmed]
 
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