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

C. Geoffrey Woods

Department of Medical Genetics

Cambridge Institute for Medical Research

Cambridge

United Kingdom

[email]@cam.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, Cambridge Institute for Medical Research, Cambridge, United Kingdom. 2005 - 2006

References

  1. Quantification of homozygosity in consanguineous individuals with autosomal recessive disease. Woods, C.G., Cox, J., Springell, K., Hampshire, D.J., Mohamed, M.D., McKibbin, M., Stern, R., Raymond, F.L., Sandford, R., Malik Sharif, S., Karbani, G., Ahmed, M., Bond, J., Clayton, D., Inglehearn, C.F. Am. J. Hum. Genet. (2006) [Pubmed]
  2. Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome. Woods, C.G., Stricker, S., Seemann, P., Stern, R., Cox, J., Sherridan, E., Roberts, E., Springell, K., Scott, S., Karbani, G., Sharif, S.M., Toomes, C., Bond, J., Kumar, D., Al-Gazali, L., Mundlos, S. Am. J. Hum. Genet. (2006) [Pubmed]
  3. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. Woods, C.G., Bond, J., Enard, W. Am. J. Hum. Genet. (2005) [Pubmed]
 
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