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

Rhonda E. Schnur

Division of Genetics

Department of Pediatrics

Cooper University Hospital/Robert Wood Johnson Medical School

Camden

USA

[email]@umdnj.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Division of Genetics, Department of Pediatrics, Cooper University Hospital/Robert Wood Johnson Medical School, Camden, USA. 2004
  • Division of Genetics, Children's Regional Hospital, Camden, NJ 08103, USA. 1998
  • Department of Pediatrics at the Children's Hospital of Philadelphia, Pennsylvania, USA. 1997

References

  1. Genodermatoses 2003-2004. Schnur, R.E. Curr. Opin. Pediatr. (2004) [Pubmed]
  2. OA1 mutations and deletions in X-linked ocular albinism. Schnur, R.E., Gao, M., Wick, P.A., Keller, M., Benke, P.J., Edwards, M.J., Grix, A.W., Hockey, A., Jung, J.H., Kidd, K.K., Kistenmacher, M., Levin, A.V., Lewis, R.A., Musarella, M.A., Nowakowski, R.W., Orlow, S.J., Pagon, R.S., Pillers, D.A., Punnett, H.H., Quinn, G.E., Tezcan, K., Wagstaff, J., Weleber, R.G. Am. J. Hum. Genet. (1998) [Pubmed]
  3. Acute lymphoblastic leukemia in a child with the CHIME neuroectodermal dysplasia syndrome. Schnur, R.E., Greenbaum, B.H., Heymann, W.R., Christensen, K., Buck, A.S., Reid, C.S. Am. J. Med. Genet. (1997) [Pubmed]
 
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