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An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

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An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome is a paper indexed in ScholarIQ from OpenAlex.

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An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome has 385 citations in the OpenAlex counts ScholarIQ stores.

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An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome has 1996 year in the ScholarIQ index.

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An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome has closed oa status in the ScholarIQ index.

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