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APA Citation
Müller, A., Soellner, L., Binder, G., Begemann, M., & Eggermann, T. (2016). no major contribution of IGF2 variants to the etiology of sporadic 11p15‐associated imprinting disorders. American journal of medical genetics, 170(1), 283–284. http://access.bl.uk/ark:/81055/vdc_100028004586.0x00000b