IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome (Q70765937)

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scientific article published on 01 May 1993
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IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
scientific article published on 01 May 1993

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    IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome (English)

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