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Q35881189-C8950137-3B12-474B-9837-8DF402DE0735
Q35881189-C8950137-3B12-474B-9837-8DF402DE0735
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http://www.wikidata.org/entity/statement/Q35881189-C8950137-3B12-474B-9837-8DF402DE0735
Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes.
P2860
Q35881189-C8950137-3B12-474B-9837-8DF402DE0735
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35881189-C8950137-3B12-474B-9837-8DF402DE0735
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wasDerivedFrom
b36eee1052c31ccae7c75ff7f0d7438938a0cc86
P2860
Loss of the maternal H19 gene induces changes in Igf2 methylation in both cis and trans