Stefan Meyer
Department of Paediatric Haematology and Oncology
Central Manchester and Manchester Children's University Hospital and Christie Hospital NHS Trusts
Manchester
UK
Name/email consistency: high
- 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)
- 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)