Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth? | Journal of Medical Genetics

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Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?

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Cite this article as:: Okamoto K, Morison IM, Reeve AE, et al

Is p57KIP2 mutation a common mechanism for Beckwith-Wiedemann syndrome or somatic overgrowth?

Journal of Medical Genetics 1998;35:86.