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APA Citation
Filges, I., Shimojima, K., Okamoto, N., Röthlisberger, B., Weber, P., Huber, A. R., Nishizawa, T., Datta, A. N., Miny, P., & Yamamoto, T. (2011). reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel–Giedion syndrome. Journal of medical genetics, 48(2), 117–122. http://access.bl.uk/ark:/81055/vdc_100136585304.0x000041