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Catherine J. Owen

Institute of Human Genetics

University of Newcastle

International Centre for Life

Central Parkway

UK

[email]@ncl.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Institute of Human Genetics, University of Newcastle, International Centre for Life, Central Parkway, UK. 2007 - 2009
  • Institute of Human Genetics and Department of Child Health, University of Newcastle upon Tyne, United Kingdom. 2003 - 2006

References

  1. Diagnosis and management of polyendocrinopathy syndromes. Owen, C.J., Cheetham, T.D. Endocrinol. Metab. Clin. North Am. (2009) [Pubmed]
  2. Analysis of the Fc receptor-like-3 (FCRL3) locus in Caucasians with autoimmune disorders suggests a complex pattern of disease association. Owen, C.J., Kelly, H., Eden, J.A., Merriman, M.E., Pearce, S.H., Merriman, T.R. J. Clin. Endocrinol. Metab. (2007) [Pubmed]
  3. Genetic association studies of the FOXP3 gene in Graves' disease and autoimmune Addison's disease in the United Kingdom population. Owen, C.J., Eden, J.A., Jennings, C.E., Wilson, V., Cheetham, T.D., Pearce, S.H. J. Mol. Endocrinol. (2006) [Pubmed]
  4. Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome. Owen, C.J., Jennings, C.E., Imrie, H., Lachaux, A., Bridges, N.A., Cheetham, T.D., Pearce, S.H. J. Clin. Endocrinol. Metab. (2003) [Pubmed]
 
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