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Botta, A., Novelli, G., Mari, A., Novelli, A., Sabani, M., Korenberg, J., Osborne, L. R., Digilio, M. C., Giannotti, A., & Dallapiccola, B. (1999). detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes. Journal of medical genetics, 36(6), 478–480. http://access.bl.uk/ark:/81055/vdc_100135144600.0x00003b