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Williams Syndrome: evidence from atypical deletions links GTF21 and GTF2IRD1, but not FZD9, with posterior cortical structure and neural functions 53rd Annual Meeting of the American-Society-of-Human-Genetics Simon, A. F., Yao, G. M., Chen, X. N., Mills, D., Rose, F. E., Salandanan, L. S., Reiss, A., Bellugi, U., Korenberg, J. R. CELL PRESS. 2003: 514–14
View details for Web of Science ID 000185599702022