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Q46641071-A71C9DCE-6740-4601-B78B-24E82C7200B6
Q46641071-A71C9DCE-6740-4601-B78B-24E82C7200B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46641071-A71C9DCE-6740-4601-B78B-24E82C7200B6
Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.
P2860
Q46641071-A71C9DCE-6740-4601-B78B-24E82C7200B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46641071-A71C9DCE-6740-4601-B78B-24E82C7200B6
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wasDerivedFrom
9df83b4833b6fbc49adf3d8ecacbc1a82e297385
P2860
Beckwith-Wiedemann syndrome caused by maternally inherited mutation of an OCT-binding motif in the IGF2/H19-imprinting control region, ICR1.