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

Frances R. Goodman

Molecular Medicine Unit

Institute of Child Health


United Kingdom


Name/email consistency: high



  • Molecular Medicine Unit, Institute of Child Health, London, United Kingdom. 2000 - 2003
  • Molecular Medicine Unit, University of Florence. 1998


  1. Congenital abnormalities of body patterning: embryology revisited. Goodman, F.R. Lancet (2003) [Pubmed]
  2. A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly. Goodman, F.R., Majewski, F., Collins, A.L., Scambler, P.J. Am. J. Hum. Genet. (2002) [Pubmed]
  3. Limb malformations and the human HOX genes. Goodman, F.R. Am. J. Med. Genet. (2002) [Pubmed]
  4. Human HOX gene mutations. Goodman, F.R., Scambler, P.J. Clin. Genet. (2001) [Pubmed]
  5. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. Goodman, F.R., Bacchelli, C., Brady, A.F., Brueton, L.A., Fryns, J.P., Mortlock, D.P., Innis, J.W., Holmes, L.B., Donnenfeld, A.E., Feingold, M., Beemer, F.A., Hennekam, R.C., Scambler, P.J. Am. J. Hum. Genet. (2000) [Pubmed]
  6. Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families. Goodman, F., Giovannucci-Uzielli, M.L., Hall, C., Reardon, W., Winter, R., Scambler, P. Am. J. Hum. Genet. (1998) [Pubmed]
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