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

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Rhonda E. Schnur

Division of Genetics

Department of Pediatrics

Cooper University Hospital/Robert Wood Johnson Medical School

Camden

USA

[email]@umdnj.edu

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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

Genodermatoses 2003-2004. Schnur, R.E. Curr. Opin. Pediatr. (2004) [Pubmed]
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]
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]