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Q33325473-FEEF3C0D-21FD-4213-B755-A2F6F892D993
Q33325473-FEEF3C0D-21FD-4213-B755-A2F6F892D993
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http://www.wikidata.org/entity/statement/Q33325473-FEEF3C0D-21FD-4213-B755-A2F6F892D993
Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.
P2860
Q33325473-FEEF3C0D-21FD-4213-B755-A2F6F892D993
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33325473-FEEF3C0D-21FD-4213-B755-A2F6F892D993
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wasDerivedFrom
772040c29ed6fa0d7014d90c4b75ae24ec54c854
P2860
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.