Cite
MLA Citation
F D Hannes et al.. “Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.” Journal of medical genetics, vol. 46, no. 4, 2009, pp. 223–232. http://access.bl.uk/ark:/81055/vdc_100135541397.0x00003d