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    K. Higashimoto, K. Jozaki, T. Kosho, K. Matsubara, T. Fuke, D. Yamada, H. Yatsuki, T. Maeda, Y. Ohtsuka, K. Nishioka, K. Joh, H. Koseki, T. Ogata, H. Soejima, 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, 2014, 86, 6
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