Cite
MLA Citation
Kosuke Izumi et al.. “Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features.” American journal of medical genetics, vol. 161, no. 12, n.d., pp. 3137–3143. http://access.bl.uk/ark:/81055/vdc_100024735862.0x000057