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

Stefan Meyer

Department of Paediatric Haematology and Oncology

Central Manchester and Manchester Children's University Hospital and Christie Hospital NHS Trusts

Manchester

UK

[email]@manchester.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Paediatric Haematology and Oncology, Central Manchester and Manchester Children's University Hospital and Christie Hospital NHS Trusts, Manchester, UK. 2006

References

  1. Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia. Meyer, S., Barber, L.M., White, D.J., Will, A.M., Birch, J.M., Kohler, J.A., Ersfeld, K., Blom, E., Joenje, H., Eden, T.O., Malcolm Taylor, G. Br. J. Haematol. (2006) [Pubmed]
  2. No evidence of significant silencing of Fanconi genes FANCF and FANCB or Nijmegen breakage syndrome gene NBS1 by DNA hyper-methylation in sporadic childhood leukaemia. Meyer, S., White, D.J., Will, A.M., Eden, T., Sim, A., Brown, R., Strathdee, G. Br. J. Haematol. (2006) [Pubmed]
 
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