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Higashimoto, K. et al. (n.d.). A novel de novo point mutation of the OCT‐binding site in the IGF2/H19‐imprinting control region in a Beckwith–Wiedemann syndrome patient. Clinical genetics. pp. 539-544. [Online].
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Higashimoto, K. et al. (n.d.). A novel de novo point mutation of the OCT‐binding site in the IGF2/H19‐imprinting control region in a Beckwith–Wiedemann syndrome patient. Clinical genetics. pp. 539-544. [Online].