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

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Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.

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References

  1. Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1. Debeer, P., Vandenbossche, L., de Ravel, T.J., Desloovere, C., De Smet, L., Huysmans, C., Thoelen, R., Vermeesch, J., Van de Ven, W.J., Fryns, J.P. Clin. Genet. (2004) [Pubmed]
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