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Charles Shaw-Smith
Wellcome Trust Sanger Institute
Hinxton
Cambridge
UK
Name/email consistency: high
- Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature. Shaw-Smith, C. Eur. J. Med. Genet (2010)
- Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Shaw-Smith, C., Pittman, A.M., Willatt, L., Martin, H., Rickman, L., Gribble, S., Curley, R., Cumming, S., Dunn, C., Kalaitzopoulos, D., Porter, K., Prigmore, E., Krepischi-Santos, A.C., Varela, M.C., Koiffmann, C.P., Lees, A.J., Rosenberg, C., Firth, H.V., de Silva, R., Carter, N.P. Nat. Genet. (2006)
