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

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Frances R. Goodman

Molecular Medicine Unit

Institute of Child Health

London

United Kingdom

[email]@hgmp.mrc.ac.uk

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Affiliations

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

References

Congenital abnormalities of body patterning: embryology revisited. Goodman, F.R. Lancet (2003) [Pubmed]
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]
Limb malformations and the human HOX genes. Goodman, F.R. Am. J. Med. Genet. (2002) [Pubmed]
Human HOX gene mutations. Goodman, F.R., Scambler, P.J. Clin. Genet. (2001) [Pubmed]
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]
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]