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

R. Scott Hansen

Department of Medicine

University of Washington

Seattle

WA 98195

USA

[email]@u.washington.edu

Name/email consistency: low

 
 
 
 
 
 
 

Affiliation

  • Department of Medicine, University of Washington, Seattle, WA 98195, USA. 1999 - 2003

References

  1. X inactivation-specific methylation of LINE-1 elements by DNMT3B: implications for the Lyon repeat hypothesis. Hansen, R.S. Hum. Mol. Genet. (2003) [Pubmed]
  2. Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant. Hansen, R.S., Stöger, R., Wijmenga, C., Stanek, A.M., Canfield, T.K., Luo, P., Matarazzo, M.R., D'Esposito, M., Feil, R., Gimelli, G., Weemaes, C.M., Laird, C.D., Gartler, S.M. Hum. Mol. Genet. (2000) [Pubmed]
  3. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. Hansen, R.S., Wijmenga, C., Luo, P., Stanek, A.M., Canfield, T.K., Weemaes, C.M., Gartler, S.M. Proc. Natl. Acad. Sci. U.S.A. (1999) [Pubmed]
 
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