Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

Source:http://linkedlifedata.com/resource/pubmed/id/11751681

Hum. Mol. Genet. 2001 Dec 15 10 26 2989-3000

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PMID
11751681