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Coldren, C. D., Lai, Z., Shragg, P., Rossi, E., Glidewell, S. C., Zuffardi, O., Mattina, T., Ivy, D. D., Curfs, L. M., Mattson, S. N., Riley, E. P., Treier, M., & Grossfeld, P. D. (2009). Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioural defects in the 11q terminal deletion disorder (Jacobsen syndrome). Neurogenetics, 10, 89-95. doi:10.1007/s10048-008-0157-x

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