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Müller, A. et al. (2016). No major contribution of IGF2 variants to the etiology of sporadic 11p15‐associated imprinting disorders. American journal of medical genetics. 170 (1), pp. 283-284. [Online].
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Müller, A. et al. (2016). No major contribution of IGF2 variants to the etiology of sporadic 11p15‐associated imprinting disorders. American journal of medical genetics. 170 (1), pp. 283-284. [Online].