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Q33678779-E2A2696E-37BB-4C32-B206-5BA30A95022D
Q33678779-E2A2696E-37BB-4C32-B206-5BA30A95022D
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http://www.wikidata.org/entity/statement/Q33678779-E2A2696E-37BB-4C32-B206-5BA30A95022D
Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.
P2860
Q33678779-E2A2696E-37BB-4C32-B206-5BA30A95022D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33678779-E2A2696E-37BB-4C32-B206-5BA30A95022D
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wasDerivedFrom
e7bea143dcc3587499f438f2411589195b2e13b8
P2860
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.