Cite

    Zarrei, M., Merico, D., Kellam, B., Engchuan, W., Scriver, T., Jokhan, R., Wilson, M. D., Parr, J., Lemire, E. G., Stavropoulos, D. J., & Scherer, S. W. (2017). a de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome. American journal of medical genetics, 173(5), 1287–1293. http://access.bl.uk/ark:/81055/vdc_100045721623.0x00000e