C. Geoffrey Woods
Department of Medical Genetics
Cambridge Institute for Medical Research
Cambridge
United Kingdom
Name/email consistency: high
- 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)
- 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)
- 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)