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Q24684284-725AA91F-BDEC-466F-B332-1564AEB7B765
Q24684284-725AA91F-BDEC-466F-B332-1564AEB7B765
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http://www.wikidata.org/entity/statement/Q24684284-725AA91F-BDEC-466F-B332-1564AEB7B765
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
P2860
Q24684284-725AA91F-BDEC-466F-B332-1564AEB7B765
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24684284-725AA91F-BDEC-466F-B332-1564AEB7B765
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type
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wasDerivedFrom
0ea619e31e43c37512acabd644261f8af2204cc5
P2860
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome.