Cite

    Douglas, J., Tatton-Brown, K., Coleman, K., Guerrero, S., Berg, J., Cole, T. R. P., FitzPatrick, D., Gillerot, Y., Hughes, H. E., Pilz, D., Raymond, F. L., Temple, I. K., Irrthum, A., Schouten, J. P., & Rahman, N. (2005). partial NSD1 deletions cause 5% of Sotos syndrome and are readily identifiable by multiplex ligation dependent probe amplification. Journal of medical genetics, 42(9), e56. http://access.bl.uk/ark:/81055/vdc_100137782039.0x000047