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APA Citation
Izumi, K., Housam, R., Kapadia, C., Stallings, V. A., Medne, L., Shaikh, T. H., Kublaoui, B. M., Zackai, E. H., & Grimberg, A. (n.d.). endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. American journal of medical genetics, 161(12), 3137–3143. http://access.bl.uk/ark:/81055/vdc_100024735862.0x000057