Authors: Osborne, LR Li, M Pober, B Chitayat, D Bodurtha, J Mandel, A Costa, T Grebe, T Cox, S Tsui, LC Scherer, SW

Citation: Lr. Osborne et al., A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome, NAT GENET, 29(3), 2001, pp. 321-325

Authors: Osborne, LR

Citation: Lr. Osborne, Williams-Beuren syndrome: Unraveling the mysteries of a microdeletion disorder, MOL GEN MET, 67(1), 1999, pp. 1-10

Authors: Osborne, LR Campbell, T Daradich, A Scherer, SW Tsui, LC

Citation: Lr. Osborne et al., Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome, GENOMICS, 57(2), 1999, pp. 279-284

Authors: Botta, A Novelli, G Mari, A Novelli, A Sabani, M Korenberg, J Osborne, LR Digilio, MC Giannotti, A Dallapiccola, B

Citation: A. Botta et al., Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes, J MED GENET, 36(6), 1999, pp. 478-480

Authors: Jadayel, DM Osborne, LR Coignet, LJA Zani, VJ Tsui, LC Scherer, SW Dyer, MJS

Citation: Dm. Jadayel et al., The BCL7 gene family: deletion of BCL7B in Williams syndrome, GENE, 224(1-2), 1998, pp. 35-44