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

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Phil J. Ancliff

Department of Haematology

University College London

United Kingdom

[email]@ucl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Haematology, University College London, United Kingdom. 2001 - 2003
  • Department of Haematology and Immunology, University College London and Great Ormond Street Children's Hospital, London, United Kingdom. 2002

References

  1. Long-term follow-up of granulocyte colony-stimulating factor receptor mutations in patients with severe congenital neutropenia: implications for leukaemogenesis and therapy. Ancliff, P.J., Gale, R.E., Liesner, R., Hann, I., Linch, D.C. Br. J. Haematol. (2003) [Pubmed]
  2. Paternal mosaicism proves the pathogenic nature of mutations in neutrophil elastase in severe congenital neutropenia. Ancliff, P.J., Gale, R.E., Watts, M.J., Liesner, R., Hann, I.M., Strobel, S., Linch, D.C. Blood (2002) [Pubmed]
  3. Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease. Ancliff, P.J., Gale, R.E., Liesner, R., Hann, I.M., Linch, D.C. Blood (2001) [Pubmed]
 
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