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Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cellsDetermination of KCNQ1OT1 and H19 methylation levels in BWS and SRS patients using methylation-sensitive high-resolution melting analysis.Monozygotic twins discordant for vascular malformations and dysregulated growth.Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndromeEpigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS)
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Q34326159-B577EE91-48FF-4CA2-8C6C-4AA26D0AB421Q34328129-B5910283-21EF-43A5-A233-F2BF4B73C6D3Q42354455-6EC95408-BE07-4976-82E1-7A7DE79488E6Q51617218-76FCEDFE-864D-44A6-988A-31A43D6E0F63Q51697360-1507AAE9-23C0-4D82-BF6F-3F27DB1E4B95Q58134227-2A526855-3CE1-4C98-85B7-874F813FBAC9Q62782884-6449D36A-98CC-44C2-B517-88E2CE5428A3
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P21
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0000-0003-4549-6655
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2000-01-01T00:00:00Z