Rhonda E. Schnur
Division of Genetics
Department of Pediatrics
Cooper University Hospital/Robert Wood Johnson Medical School
Camden
USA
Name/email consistency: high
- Genodermatoses 2003-2004. Schnur, R.E. Curr. Opin. Pediatr. (2004)
- 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)
- 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)